Label: 4056 FIRST AID KIT kit
4068 FIRST AID KIT kit
4088 FIRST AID KIT kit
4089 FIRST AID KIT kit
4081 FIRST AID KIT kit
4090 FIRST AID KIT kit
4083 FIRST AID KIT kit
4087 FIRST AID KIT kit
4082 FIRST AID KIT kit
4084 FIRST AID KIT kit
4085 FIRST AID KIT kit
4086 FIRST AID KIT kit
-
NDC Code(s):
0498-0100-01,
0498-0730-01,
0498-2001-01,
0498-4056-01, view more0498-4068-01, 0498-4081-01, 0498-4082-01, 0498-4083-01, 0498-4084-01, 0498-4085-01, 0498-4086-01, 0498-4087-01, 0498-4088-01, 0498-4089-01, 0498-4090-01
- Packager: Honeywell Safety Products USA, INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated January 22, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
-
Warnings
For external use only- Obtain immediate medical treatment for all open wounds in or near the eyes. To avoid contamination, do not touch tip of container to any surface. Do not reuse. Once opened, discard.
Do not use
- if solution changes color or becomes cloudy
- if you have open wounds in or near the eyes, get medical help right away
- Directions
- Inactive Ingredients
- Questions?
- First Aid Burn Cream Active ingredient
- First Aid Burn Cream Purpose
- First Aid Burn Cream Uses
- First Aid Burn Cream Warnings
- First Aid Burn Cream Directions
- Other information
- Inactive ingredients
- Questions
- BZK Antiseptic Wipe Active ingredient
- BZK Purpose
- BZK Uses
-
BZK
Warnings
For external use only
BZK
Do not use- in the eyes or over large areas of the body
- on mucous membranes
- on irritated skin
- in case of deep puncture wounds, animal bites or serious burns, consult a doctor
- longer than 1 week unless directed by a doctor
- BZK Directions
- BZK Other information
- BZK Inactive ingredients
- BZK Questions
- Aypanal Active igredient
- Aypanal Purpose
- Aypanal Uses
-
Aypanal
Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take: more than 4,000 mg in 24 hours, which is the maximum daily amount - child takes
Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:
skin reddening
blisters
rash -
Aypanal
Directions
- do not take more than directed (see overdose warning) adults and children 12 years of age or older
- take two tablets every 4-6 hours while symptoms last
- do not take more than directed (see overdose warning)
adults and children 12 years of age or older
- take two tablets every 4-6 hours while symptoms last
- do not take more than 12 tablets in 24 hours
- children 6 to under 12 years of age
- take 1 tablet every 4-6 hours while symptoms last
- do not take more than 5 tablets in 24 hours
- children under 6 years
- consult a doctor
- Aypanal Other information
- Aypanal Inactive ingredients
- Aypanal Questions or Comments?
- Sting Relief Active ingredient
- Sting Relief Purpose
- Sting Relief Uses
- Sting Relief Warnings
- Sting Relief Directions
- Sting Relief Inactive ingredients
- Sting relief Questions or Comments
- Neomycin Antibiotic Ointment Active ingredient
- Neomycin Antibiotic Ointment Purpose
- Neomycin Antibiotic Ointment Uses
- Neomycin Antibiotic Ointment Warnings
- Neomycin Antibiotic Ointment Directions
- Neomycin Antibiotic Ointment Other information
- Neomycin Antibiotic Ointment Inactive ingredient
- Neomycin Antibiotic Ointment Questions
-
4056
Z019851 Kit Contents
1 TWEEZER PLASTICS 4"
1 FIRST AID GUIDE ASHI
2 GAUZE CLEAN-WRAP BDGE N/S 2"
1 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 CPR FILTERSHIELD 77-100
1 BAGGED COMP MISC
1 BUFF EYEWASH 1oz
1 SCISSOR BDGE 4" RED PLS HDL
2 PR LRG NITRILE GLVES ZIP BAG
2 1" X 3" PLASTIC BANDS 16/BAG
2 TAPE ADHESIVE 1/2 X 2.5 125133
1 ADH BNDG PLASTIC EX-LG 4"X 2"
1 TRI BNDG NON WOVEN 40"X40"X56"
1 COLD PACK UNIT 4"X6" BULK
1 GAUZE PADS 2"X2" 12PLY
1 EYE PADS STD OVAL STERILE
4 GAUZE PADS 3"X3" 12PLY
3 WOVEN FINGERTIP BANDAGE 2"
2 WOVEN KNUCKLE BANDAGE
-
4068
SF00001232 Kit Contents
1 1X3 PLASTIC 100/BOX
1 TWEEZER PLASTICS 4"
1 FIRST AID GUIDE ASHI
3 GAUZE CLEAN-WRAP BDGE N/S 2"
2 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 CO-FLEX BANDAGE 2"X 5YDS TAN
1 CPR FILTERSHIELD 77-100
2 BAGGED COMP MISC
1 1OZ. EYEWASH
1 SCISSOR BDGE 4" RED PLS HDL
1 LABEL NORTH CONTENTS 8X8 ID B
1 LABEL RAPID PICS 24U/50P
2 PR LRG NITRILE GLVES ZIP BAG
2 TAPE ADHESIVE 1/2 X 2.5 125133
2 ADH BNDG PLASTIC EX-LG 4"X 2"
1 KIT PP 24 UNIT FA
1 BAG ZIPPER POLY 6 X 6 2 MIL -
4081
Z019702-0002L Kit Contents
1 TWEEZER PLASTICS 4"
1 FIRST AID GUIDE ASHI
2 GAUZE CLEAN-WRAP BDGE N/S 2"
1 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 CPR FILTERSHIELD 77-100
1 BAGGED COMP MISC
1 1 OZ, BUFF EYEWASH
1 SCISSOR BDGE 4" RED PLS HDL
1 2 PR LRG NITRILE GLVES ZIP BAG
2 1" X 3" PLASTIC BANDS 16/BAG
2 TAPE ADHESIVE 1/2 X 2.5 125133
1 ADH BNDG PLASTIC EX-LG 4"X 2"
1 KIT, PP 16 UNIT FA
1 LBL 25P CVR NORTH ID B
1 TRI BNDG NON WOVEN 40"X40"X56"
1 COLD PACK UNIT 4"X6" BULK
1 GAUZE PADS 2"X2" 12PLY
1 EYE PADS STD OVAL STERILE
4 GAUZE PADS 3"X3" 12PLY
3 WOVEN FINGERTIP BANDAGE 2"
2 WOVEN KNUCKLE BANDAGE -
4082
Z019704-0003L Kit Contents
1 1X3 PLASTIC 100/BOX
1 TWEEZER PLASTICS 4"
1 FIRST AID GUIDE ASHI
3 GAUZE CLEAN-WRAP BDGE N/S 2"
2 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 CO-FLEX BANDAGE 2"X 5YDS TAN
1 CPR FILTERSHIELD 77-100
2 BAGGED COMP MISC
1 1 OZ. EYEWASH
1 SCISSOR BDGE 4" RED PLS HDL
1 2 PR LRG NITRILE GLVES ZIP BAG
2 TAPE ADHESIVE 1/2 X 2.5 125133
2 ADH BNDG PLASTIC EX-LG 4"X 2"
1 KIT PP 24 UNIT FA
1 LBL 50P CVR NORTH ID B
1 TRI BNDG NON WOVEN 40"X40"X56"
2 COLD PACK UNIT 4"X6" BULK
8 GAUZE PADS 2"X2" 12PLY
2 EYE PADS STD OVAL STERILE
4 GAUZE PADS 3"X3" 12PLY
4 WOVEN FINGERTIP BANDAGE 2"
3 WOVEN KNUCKLE BANDAGE -
4083
019702-0002L Kit Contents
1 TWEEZER PLASTICS 4"
1 FIRST AID GUIDE ASHI
2 GAUZE CLEAN-WRAP BDGE N/S 2"
1 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 CPR FILTERSHIELD 77-100
1 BAGGED COMP MISC
1 1 OZ. EYEWASH
1 SCISSOR BDGE 4" RED PLS HDL
1 2 PR LRG NITRILE GLVES ZIP BAG
2 1" X 3" PLASTIC BANDS 16/BAG
2 TAPE ADHESIVE 1/2 X 2.5 125133
1 ADH BNDG PLASTIC EX-LG 4"X 2"
1 KIT, PP 16 UNIT FA
1 LBL 25P CVR NORTH ID B
1 TRI BNDG NON WOVEN 40"X40"X56"
1 COLD PACK UNIT 4"X6" BULK
1 GAUZE PADS 2"X2" 12PLY
1 EYE PADS STD OVAL STERILE
4 GAUZE PADS 3"X3" 12PLY
3 WOVEN FINGERTIP BANDAGE 2"
2 WOVEN KNUCKLE BANDAGE -
4084
019703-0002L Kit Contents
1 GAUZE PADS, 3" X 3", 4 PER
1 TWEEZER PLASTICS 4"
1 FIRST AID GUIDE ASHI
2 GAUZE CLEAN-WRAP BDGE N/S 2"
1 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 CPR FILTERSHIELD 77-100
1 BAGGED COMP MISC
1 1 OZ.EYEWASH
1 SCISSOR BDGE 4" RED PLS HDL
1 2 PR LRG NITRILE GLVES ZIP BAG
2 1" X 3" PLASTIC BANDS 16/BAG
2 TAPE ADHESIVE 1/2 X 2.5 125133
1 ADH BNDG PLASTIC EX-LG 4"X 2"
1 KIT STL 16 UN (HORIZONTAL)1 LBL CONTENTS ANSI Z308.1-2009 REV B
1 LBL 25P CVR NORTH ID B1 TRI BNDG NON WOVEN 40"X40"X56"
1 COLD PACK UNIT 4"X6" BULK
4 GAUZE PADS 2"X2" 12PLY
1 EYE PADS STD OVAL STERILE
3 WOVEN FINGERTIP BANDAGE 2"
2 WOVEN KNUCKLE BANDAGE -
4085
019703-4503 Kit Contents
1 TWEEZER PLASTICS 4"
1 FIRST AID GUIDE ASHI
2 GAUZE CLEAN-WRAP BDGE N/S 2"
1 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 CPR FILTERSHIELD 77-100
1 BAGGED COMP MISC
1 1 OZ.EYEWASH
1 SCISSOR BDGE 4" RED PLS HDL
1 2 PR LRG NITRILE GLVES ZIP BAG
2 TAPE ADHESIVE 1/2 X 2.5 125133
1 ADH BNDG PLASTIC EX-LG 4"X 2"
1 KIT STL 16 UN (HORIZONTAL)
1 1 LBL 25P CVR NORTH ID B
1 TRI BNDG NON WOVEN 40"X40"X56"
1 COLD PACK UNIT 4"X6" BULK
4 GAUZE PADS 2"X2" 12PLY
1 EYE PADS STD OVAL STERILE
1 GAUZE PADS 3"X3" 12PLY
30 PLASTIC BANDAGE 1" X 3"
3 WOVEN FINGERTIP BANDAGE 2"
2 WOVEN KNUCKLE BANDAGE -
4086
019704-0003L Kit Contents
1 1X3 PLASTIC 100/BOX
1 GAUZE PADS, 3" X 3", 4 PER
1 TWEEZER PLASTICS 4"
1 FIRST AID GUIDE ASHI
3 GAUZE CLEAN-WRAP BDGE N/S 2"
2 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 CO-FLEX BANDAGE 2"X 5YDS TAN
1 CPR FILTERSHIELD 77-100
2 BAGGED COMP MISC
1 1 OZ. EYEWASH
1 SCISSOR BDGE 4" RED PLS HDL
1 LABEL NORTH CONTENTS 8X8 ID B
1 2 PR LRG NITRILE GLVES ZIP BAG
2 TAPE ADHESIVE 1/2 X 2.5 125133
2 ADH BNDG PLASTIC EX-LG 4"X 2"
1 KIT PP 24 UNIT FA
1 LBL CONTENTS ANSI Z308.1-2009 REV B
1 LBL 50P CVR NORTH ID B
1 TRI BNDG NON WOVEN 40"X40"X56"
2 COLD PACK UNIT 4"X6" BULK
10 GAUZE PADS 2"X2" 12PLY
2 EYE PADS STD OVAL STERILE
4 WOVEN FINGERTIP BANDAGE 2"
3 WOVEN KNUCKLE BANDAGE -
4087
019704-4504 Kit Contents
1 1X3 PLASTIC 100/BOX
1 TWEEZER PLASTICS 4"
1 FIRST AID GUIDE ASHI
3 GAUZE CLEAN-WRAP BDGE N/S 2"
2 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 CO-FLEX BANDAGE 2"X 5YDS TAN
1 CPR FILTERSHIELD 77-100
2 BAGGED COMP MISC
1 1 OZ.EYEWASH
1 SCISSOR BDGE 4" RED PLS HDL
1 2 PR LRG NITRILE GLVES ZIP BAG
2 TAPE ADHESIVE 1/2 X 2.5 125133
2 ADH BNDG PLASTIC EX-LG 4"X 2"
1 KIT PP 24 UNIT FA
1 LBL 50P CVR NORTH ID B
1 TRI BNDG NON WOVEN 40"X40"X56"
2 COLD PACK UNIT 4"X6" BULK
10 GAUZE PADS 2"X2" 12PLY
2 EYE PADS STD OVAL STERILE
2 GAUZE PADS 3"X3" 12PLY
4 WOVEN FINGERTIP BANDAGE 2"
3 WOVEN KNUCKLE BANDAGE -
4088
019705-4505 Kit Contents
1 1" X 3" PLAS 100/BOX
1 TWEEZER PLASTICS 4"
1 FIRST AID GUIDE ASHI
3 GAUZE CLEAN-WRAP BDGE N/S 2"
2 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 CO-FLEX BANDAGE 2"X 5YDS TAN
1 CPR FILTERSHIELD 77-100
2 BAGGED COMP MISC
1 1 OZ.EYEWASH
1 SCISSOR BDGE 4" RED PLS HDL
1 2 PR LRG NITRILE GLVES ZIP BAG
2 TAPE ADHESIVE 1/2 X 2.5 125133
2 ADH BNDG PLASTIC EX-LG 4"X 2"
1 KIT STL 24 UN WHITE 01
1 LBL 50P CVR NORTH ID B
1 TRI BNDG NON WOVEN 40"X40"X56"
2 COLD PACK UNIT 4"X6" BULK
10 GAUZE PADS 2"X2" 12PLY
2 EYE PADS STD OVAL STERILE
2 GAUZE PADS 3"X3" 12PLY
4 WOVEN FINGERTIP BANDAGE 2"
3 WOVEN KNUCKLE BANDAGE -
4089
Z019707-0004L Kit Contents
1 1X3 PLASTIC 100/BOX
1 WIRE SPLINT 1 PER
1 TWEEZER PLASTICS 4"
1 FIRST AID GUIDE ASHI
4 GAUZE CLEAN-WRAP BDGE N/S 2"
2 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 GZE PADS STERILE 2"X 2" 10'S
1 CO-FLEX BANDAGE 2"X 5YDS TAN
1 CPR FILTERSHIELD 77-100
2 BAGGED COMP MISC
1 1 OZ. EYEWASH
1 SCISSOR BDGE 4" RED PLS HDL
1 5 PR LRG NITRILE GLVES ZIP BAG
3 TAPE ADHESIVE 1/2 X 2.5 125133
3 ADH BNDG PLASTIC EX-LG 4"X 2"
1 KIT STL 36 UN WHT 01 HOR SHELF
1 LBL 75P CVR NORTH ID B
1 BAG ZIPPER POLY 6 X 6 2 MIL
1 TRI BNDG NON WOVEN 40"X40"X56"
2 COLD PACK UNIT 4"X6" BULK
3 EYE PADS STD OVAL STERILE
10 GAUZE PADS 3"X3" 12PLY
8 WOVEN FINGERTIP BANDAGE 2"
6 WOVEN KNUCKLE BANDAGE -
4090
019706-0004L Kit Contents
1 1X3 PLASTIC 100/BOX
1 WIRE SPLINT 1 PER
1 TWEEZER PLASTICS 4"
1 FIRST AID GUIDE ASHI
4 GAUZE CLEAN-WRAP BDGE N/S 2"
2 GAUZE CLEAN-WRAP BDGE N/S 3"
1 ABD COMBINE PAD 5" X 9"
1 GZE PADS STERILE 2"X 2" 10'S
1 CO-FLEX BANDAGE 2"X 5YDS TAN
1 CPR FILTERSHIELD 77-100
2 BAGGED COMP MISC
2 1 OZ. EYEWASH
1 SCISSOR BDGE 4" RED PLS HDL
1 5 PR LRG NITRILE GLVES ZIP BAG
3 TAPE ADHESIVE 1/2 X 2.5 125133
3 ADH BNDG PLASTIC EX-LG 4"X 2"
1 KIT 36 UNIT PLASTIC
1 LBL CONTENTS ANSI Z308.1-2009 REV B
1 LBL 75P CVR NORTH ID B
1 TRI BNDG NON WOVEN 40"X40"X56"
2 COLD PACK UNIT 4"X6" BULK
3 EYE PADS STD OVAL STERILE
10 GAUZE PADS 3"X3" 12PLY
8 WOVEN FINGERTIP BANDAGE 2"
6 WOVEN KNUCKLE BANDAGE - Eye Wash Package label
- First Aid Burn Cream Principal Display Panel
- BZK Principal Display Panel
- Aypanal Principal Display Panel
- Sting Relief Principal Display Panel
- Neomycin Antibiotic Ointment Principal Display Panel
- 4056 Kit Label Z01985 Kit Label
- 4068 Kit Label SF00001232
- 4081 Kit Label Z019702-0002L
- 4082 Kit Label Z019704-0003L
- 4083 Kit Label 019702-0002L
- 4084 Kit Label 019703-0002L
- 4085 Kit Lael 019703-4503
- 4086 Kit Label 019704-0003L
- 4087 Kit Label 019704-4504
- 4088 Kit Label 019705-4505
- 4089 Kit Label Z019707-0004L
- 4090 Kit Label 019706-0004L
-
INGREDIENTS AND APPEARANCE
4056 FIRST AID KITÂ
4056 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4056 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4056-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE 30 mL Part 2 3 PACKET 6 Part 3 6 POUCH 2.4 mL Part 4 10 PACKET 9 g Part 5 10 PACKET 9 g Part 6 10 PACKET 14 mL Part 1 of 6 EYESALINE EMERGENCY EYEWASHÂ
purified water liquidProduct Information Item Code (Source) NDC:0498-0100 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 98.6 mL  in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0100-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M018 12/18/2018 01/08/2024 Part 2 of 6 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 01/08/2024 Part 3 of 6 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 01/08/2024 Part 4 of 6 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 01/08/2024 Part 5 of 6 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 6 of 6 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 4068 FIRST AID KITÂ
4068 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4068 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4068-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE 30 mL Part 2 6 PACKET 12 Part 3 12 POUCH 4.8 mL Part 4 20 PACKET 18 g Part 5 20 PACKET 18 g Part 6 20 PACKET 28 mL Part 1 of 6 EYESALINE EMERGENCY EYEWASHÂ
purified water liquidProduct Information Item Code (Source) NDC:0498-0100 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 98.6 mL  in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0100-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M018 12/18/2018 Part 2 of 6 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 3 of 6 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 4 of 6 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g Inactive Ingredients Ingredient Name Strength EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 5 of 6 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 6 of 6 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 4088 FIRST AID KITÂ
4088 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4088 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4088-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE 30 mL Part 2 6 PACKET 12 Part 3 12 POUCH 4.8 mL Part 4 20 PACKET 18 g Part 5 20 PACKET 18 g Part 6 20 PACKET 28 mL Part 1 of 6 EYESALINE EMERGENCY EYEWASHÂ
purified water liquidProduct Information Item Code (Source) NDC:0498-0100 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 98.6 mL  in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0100-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M018 12/18/2018 Part 2 of 6 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength POVIDONE (UNII: FZ989GH94E)  STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 3 of 6 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 4 of 6 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g Inactive Ingredients Ingredient Name Strength LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 5 of 6 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 6 of 6 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 4089 FIRST AID KITÂ
4089 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4089 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4089-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 2 BOTTLE 60 mL Part 2 6 PACKET 12 Part 3 12 POUCH 4.8 mL Part 4 20 PACKET 18 g Part 5 20 PACKET 18 g Part 6 20 PACKET 28 mL Part 1 of 6 EYESALINE EMERGENCY EYEWASHÂ
purified water liquidProduct Information Item Code (Source) NDC:0498-0100 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 98.6 mL  in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0100-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M018 12/18/2018 Part 2 of 6 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 3 of 6 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 4 of 6 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 5 of 6 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 6 of 6 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 4081 FIRST AID KITÂ
4081 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4081 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4081-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 10 PACKET 9 g Part 2 1 BOTTLE 30 mL Part 3 10 PACKET 9 g Part 4 10 PACKET 14 mL Part 5 3 PACKET 6 Part 6 6 POUCH 2.4 mL Part 1 of 6 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 2 of 6 EYESALINE EMERGENCY EYEWASHÂ
purified water liquidProduct Information Item Code (Source) NDC:0498-0100 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 98.6 mL  in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0100-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/18/2018 Part 3 of 6 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 4 of 6 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Part 5 of 6 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 6 of 6 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 4090 FIRST AID KITÂ
4090 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4090 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4090-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 2 BOTTLE 60 mL Part 2 6 PACKET 12 Part 3 12 POUCH 4.8 mL Part 4 20 PACKET 18 g Part 5 20 PACKET 18 g Part 6 20 PACKET 28 mL Part 1 of 6 EYESALINE EMERGENCY EYEWASHÂ
purified water liquidProduct Information Item Code (Source) NDC:0498-0100 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 98.6 mL  in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0100-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M018 12/18/2018 Part 2 of 6 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 3 of 6 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 4 of 6 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 5 of 6 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 6 of 6 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 4083 FIRST AID KITÂ
4083 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4083 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4083-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE 30 mL Part 2 3 PACKET 6 Part 3 6 POUCH 2.4 mL Part 4 10 PACKET 9 g Part 5 10 PACKET 9 g Part 6 10 PACKET 14 mL Part 1 of 6 EYESALINE EMERGENCY EYEWASHÂ
purified water liquidProduct Information Item Code (Source) NDC:0498-0100 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 98.6 mL  in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0100-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M018 12/18/2018 Part 2 of 6 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 3 of 6 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 4 of 6 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 5 of 6 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 6 of 6 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 4087 FIRST AID KITÂ
4087 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4087 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4087-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 6 PACKET 12 Part 2 12 POUCH 4.8 mL Part 3 20 PACKET 18 g Part 4 20 PACKET 18 g Part 5 20 PACKET 28 mL Part 6 1 BOTTLE 30 mL Part 1 of 6 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 2 of 6 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 3 of 6 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g Inactive Ingredients Ingredient Name Strength PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 4 of 6 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 5 of 6 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Part 6 of 6 EYESALINE EMERGENCY EYEWASHÂ
purified water liquidProduct Information Item Code (Source) NDC:0498-0100 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 98.6 mL  in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0100-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M018 12/18/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 4082 FIRST AID KITÂ
4082 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4082 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4082-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE 30 mL Part 2 6 PACKET 12 Part 3 12 POUCH 4.8 mL Part 4 20 PACKET 18 g Part 5 20 PACKET 18 g Part 6 20 PACKET 28 mL Part 1 of 6 EYESALINE EMERGENCY EYEWASHÂ
purified water liquidProduct Information Item Code (Source) NDC:0498-0100 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 98.6 mL  in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0100-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M018 12/18/2018 Part 2 of 6 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 3 of 6 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 4 of 6 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 5 of 6 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 6 of 6 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 4084 FIRST AID KITÂ
4084 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4084 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4084-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE 30 mL Part 2 3 PACKET 6 Part 3 6 POUCH 2.4 mL Part 4 10 PACKET 9 g Part 5 10 PACKET 9 g Part 6 10 PACKET 14 mL Part 1 of 6 EYESALINE EMERGENCY EYEWASHÂ
purified water liquidProduct Information Item Code (Source) NDC:0498-0100 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 98.6 mL  in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0100-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M018 12/18/2018 Part 2 of 6 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 3 of 6 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 4 of 6 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 5 of 6 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 6 of 6 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 4085 FIRST AID KITÂ
4085 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4085 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4085-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE 30 mL Part 2 3 PACKET 6 Part 3 6 POUCH 2.4 mL Part 4 10 PACKET 9 g Part 5 10 PACKET 9 g Part 6 10 PACKET 14 mL Part 1 of 6 EYESALINE EMERGENCY EYEWASHÂ
purified water liquidProduct Information Item Code (Source) NDC:0498-0100 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 98.6 mL  in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0100-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M018 12/18/2018 Part 2 of 6 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 3 of 6 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 4 of 6 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 5 of 6 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 6 of 6 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 4086 FIRST AID KITÂ
4086 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4086 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4086-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 10/18/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE 30 mL Part 2 6 PACKET 12 Part 3 12 POUCH 4.8 mL Part 4 20 PACKET 18 g Part 5 20 PACKET 18 g Part 6 20 PACKET 28 mL Part 1 of 6 EYESALINE EMERGENCY EYEWASHÂ
purified water liquidProduct Information Item Code (Source) NDC:0498-0100 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 98.6 mL  in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0100-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M018 12/18/2018 Part 2 of 6 AYPANAL NON-ASPIRINÂ
acetaminophen tabletProduct Information Item Code (Source) NDC:0498-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  STARCH, CORN (UNII: O8232NY3SJ)  POVIDONE (UNII: FZ989GH94E)  Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code circle;U Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-2001-01 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2012 Part 3 of 6 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct Information Item Code (Source) NDC:0498-0733 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  MENTHOL (UNII: L7T10EIP3A)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.4 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/23/2017 Part 4 of 6 FIRST AID BURNÂ
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Item Code (Source) NDC:0498-0903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  WATER (UNII: 059QF0KO0R)  STEARIC ACID (UNII: 4ELV7Z65AP)  METHYLPARABEN (UNII: A2I8C7HI9T)  CETYL ALCOHOL (UNII: 936JST6JCN)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  PEG-100 STEARATE (UNII: YD01N1999R)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/20/2017 Part 5 of 6 NEOMYCINÂ
antibiotic ointmentProduct Information Item Code (Source) NDC:0498-0730 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0730-01 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/31/2010 Part 6 of 6 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct Information Item Code (Source) NDC:0498-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 1.4 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 10/18/2019 Labeler - Honeywell Safety Products USA, INC (118768815)