Label: 4318 FIRST AID KIT- 4318 first aid kit
4319 FIRST AID KIT- 4319 first aid kit
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NDC Code(s):
0498-0100-01,
0498-0121-00,
0498-0203-00,
0498-0501-00, view more0498-0733-00, 0498-0750-35, 0498-4318-01, 0498-4319-01
- 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 December 30, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Burn Jel Active ingredient
- Burn Jel Purpose
- Burn Jel Uses
- Burn Jel Warnings
- Burn JEl Directions
- Burn Jel Other information
- Burn Jel Inactive ingredients
- Burn Jel Questions
- Triple Active ingredient
- Triple Purpose
- Triple Uses
-
Triple
Warnings
For external use only
Allergy alert: do not use if you are allergic to any of the ingredients
Do not use
- in the eyes
- over large areas of the body
- Ask a doctor before use if you have
- a deep or puncture wounds
- animal bites
- serious burns
- Triple Directions
- Triple Other information
- Triple Inactive ingredient
- Triple Questions?
- Sting Relief Active ingredient (in each wipe)
- Sting Relief Purposse
- Sting Relief Uses
- Sting Relief Warnings
- Sting Relief Directions
- Sting Relief Inactive ingredients
- Sting Relief Questions or Comments?
- Eyewash Active ingredient
- Eyewassh Purpose
- Eyewash Uses
-
Eyewash
Warnings
For external use only
- Obtain immediate medical treatment for all open wounds in or near 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.
- Eyeash Directions
- Eyewash Inactive ingredients
- Eyeash Questions
- Hydrocortisone Active ingredient (in each gram)
- Hydrcortisone Purpose
- Hydrocortisone Uses
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Hydrocortisone
Warnings
For external use onlyWhen using the product
- avoid contact with eyes
- do not begin use of any other hydrocortisone product unless you have consulted a doctor
- do not use for the treatment of diaper rash
- Hydrocortisone Directions
- Hydrocortisone Other information
- Hydrocortisone Inactive ingredients
- Hydrocortisone Questions or Comments?
- PVP Active ingredient
- PVP Purpose
- PVP Uses
- PVP Warnings
- PVP Directions
- PVP Other information
- PVP Inactive ingredients
- BZK Active ingredient
- BZK Purpose
- BZK Uses
- BZK Warnings
- BZK Directions
- BZK Other information
- BZK Inactive ingredient
- BZK Questions
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4318
SF00004559 Kit Contents
1 TRIPLE ANTIBIOTIC 10 PER
1 TRIANGULAR BDG, NON-STERILE
1 GAUZE PADS, 3" X 3", 4 PER
1 ADH TAPE, .5" X 2.5 YD, 2 PER
1 GAUZE COMP, 1 SQ YARD, 1 PER
1 ADHESIVE BDG,PLSTIC,1"X3"16PER
1 1 OZ EYE WASH W/PADS & STRIPS
1 BURN JEL 1/8 OZ, 6 PER
1 HYDROCORTISON,1.O%,1/32 OZ,10P
1 PVP IODINE WIPES 10 PER
1 BIOHAZARD BAG/SCRAPER BBP
1 ANTIMCRBL ANTSPTC TWLETTS 6PER
1 FIRST AID GUIDE ASHI
1 MICROSHIELD BAGGED 72-151
LBL STOCK 6-3/8"X4"
1 LBL STOCK 3"x1-7/8"
2 PR LRG NITRILE GLVES ZIP BAG
1 KIT STL 16 UN (HORIZONTAL)
1 STING WIPES 10
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4319
SF00004560 kit contents
1 TRIPLE ANTIBIOTIC 10 PER
1 TRIANGULAR BDG, NON-STERILE
1 GAUZE PADS, 3" X 3", 4 PER
1 ADH TAPE, .5" X 2.5 YD, 2 PER
1 GAUZE COMP, 1 SQ YARD, 1 PER
1 ADHESIVE BDG,PLSTIC,1"X3"16PER
1 ADH BAND, EXTRA LARGE, 6 PER
1 1 OZ EYE WASH W/PADS & STRIPS
1 BURN JEL 1/8 OZ, 6 PER
1 WATER JEL DRESSING 4" X 4"
1 WATER JEL DRESSING,2" X 6"
1 HYDROCORTISON,1.O%,1/32 OZ,10P
1 PVP IODINE WIPES 10 PER
1 STING RELIEF WIPES 10 PER BOX
1 BIOHAZARD BAG/SCRAPER BBP
1 ANTIMCRBL ANTSPTC TWLETTS 6PER
1 FIRST AID GUIDE ASHI
1 EMERGENCY SURVIVAL BLANKET
1 MICROSHIELD BAGGED 72-151
1 BANDAGE COMP 4" W/TELFA PAD 1
LBL STOCK 6-3/8"X4"
LBL STOCK 4"X2-7/8"
1 LBL STOCK 3"x1-7/8"
2 PR LRG NITRILE GLVES ZIP BAG
1 WATER JEL BURN DRESSING 4 X 16
1 KIT STL 36 UN WHT 01 HOR SHELF
1 COLD PACK UNIT 4"X6" BULK
1 TELFA PADS 2"X 3" 4
- Burn Jel Principal Display Panel
- Triple Principal Display Panel
- Sting Relief Principal Display Panel
- Eyewash Principal Display Panel
- Hydrocortisone Principal Display Panel
- PVP Principal Display Panel
- BZK Principal Display Panel
- 4318 Kit Label SF00004559
- 4319 Kit Label SF00004560
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INGREDIENTS AND APPEARANCE
4318 FIRST AID KITÂ
4318 first aid kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4318 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4318-01 1 in 1 KIT 09/13/2018 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 10 PACKET 9 g Part 2 6 PACKET 21 g Part 3 1 BOTTLE 30 mL Part 4 10 PACKET 9 g Part 5 6 PACKET 8.4 mL Part 6 10 POUCH 4 mL Part 7 10 PACKET 9 g Part 8 10 POUCH 3 mL Part 1 of 8 HYDROCORTISONEÂ
anti-itch creamProduct Information Item Code (Source) NDC:0498-0801 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE ACETATE (UNII: 3X7931PO74) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE ACETATE 1 g  in 100 g Inactive Ingredients Ingredient Name Strength LIGHT MINERAL OIL (UNII: N6K5787QVP)  POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  CETYL ALCOHOL (UNII: 936JST6JCN)  METHYLPARABEN (UNII: A2I8C7HI9T)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  EDETATE DISODIUM (UNII: 7FLD91C86K)  STEARIC ACID (UNII: 4ELV7Z65AP)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  TROLAMINE (UNII: 9O3K93S3TK)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  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 OTC monograph not final part348 10/15/2019 Part 2 of 8 BURN JELÂ
gel for burns gelProduct Information Item Code (Source) NDC:0498-0203 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 2 g  in 100 g Inactive Ingredients Ingredient Name Strength TEA TREE OIL (UNII: VIF565UC2G)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  METHYLPARABEN (UNII: A2I8C7HI9T)  EDETATE DISODIUM (UNII: 7FLD91C86K)  GLYCERIN (UNII: PDC6A3C0OX)  TROLAMINE (UNII: 9O3K93S3TK)  CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  OCTOXYNOL-9 (UNII: 7JPC6Y25QS)  DIPROPYLENE GLYCOL (UNII: E107L85C40)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0203-00 3.5 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 OTC monograph not final part348 09/19/2018 Part 3 of 8 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 PHOSPHATE, DIBASIC (UNII: GR686LBA74)  SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  SODIUM CHLORIDE (UNII: 451W47IQ8X)  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 final part349 12/18/2018 Part 4 of 8 TRIPLE ANTIBIOTICÂ
bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointmentProduct Information Item Code (Source) NDC:0498-0750 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 5000 [iU]  in 1 g BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 400 [iU]  in 1 g NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Product Characteristics Color white Score     Shape Size Flavor Imprint Code Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0750-35 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 OTC monograph final part333B 09/19/2018 Part 5 of 8 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 NDC:0498-0501-00 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 OTC monograph not final part333E 12/22/2017 Part 6 of 8 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 NDC:0498-0733-00 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 OTC monograph not final part348 12/23/2017 Part 7 of 8 HYDROCORTISONEÂ
anti-itch cream ointmentProduct Information Item Code (Source) NDC:0498-0800 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE ACETATE (UNII: 3X7931PO74) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE ACETATE 1 g  in 100 g Inactive Ingredients Ingredient Name Strength LIGHT MINERAL OIL (UNII: N6K5787QVP)  POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  CETYL ALCOHOL (UNII: 936JST6JCN)  METHYLPARABEN (UNII: A2I8C7HI9T)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  EDETATE DISODIUM (UNII: 7FLD91C86K)  STEARIC ACID (UNII: 4ELV7Z65AP)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  TROLAMINE (UNII: 9O3K93S3TK)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  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 OTC monograph not final part348 03/06/2013 10/15/2019 Part 8 of 8 PVP IODINE WIPEÂ
povidone-iodine 10% swabProduct Information Item Code (Source) NDC:0498-0121 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE 10 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  NONOXYNOL-9 (UNII: 48Q180SH9T)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0121-00 0.3 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 09/18/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/13/2018 4319 FIRST AID KITÂ
4319 first aid kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4319 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4319-01 1 in 1 KIT 09/13/2018 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 10 PACKET 9 g Part 2 6 PACKET 21 g Part 3 1 BOTTLE 30 mL Part 4 10 PACKET 9 g Part 5 6 PACKET 8.4 mL Part 6 10 POUCH 4 mL Part 7 10 PACKET 9 g Part 8 10 POUCH 3 mL Part 1 of 8 HYDROCORTISONEÂ
anti-itch creamProduct Information Item Code (Source) NDC:0498-0801 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE ACETATE (UNII: 3X7931PO74) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE ACETATE 1 g  in 100 g Inactive Ingredients Ingredient Name Strength LIGHT MINERAL OIL (UNII: N6K5787QVP)  POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  CETYL ALCOHOL (UNII: 936JST6JCN)  METHYLPARABEN (UNII: A2I8C7HI9T)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  EDETATE DISODIUM (UNII: 7FLD91C86K)  STEARIC ACID (UNII: 4ELV7Z65AP)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  TROLAMINE (UNII: 9O3K93S3TK)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  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 OTC monograph not final part348 10/15/2019 Part 2 of 8 BURN JELÂ
gel for burns gelProduct Information Item Code (Source) NDC:0498-0203 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 2 g  in 100 g Inactive Ingredients Ingredient Name Strength TEA TREE OIL (UNII: VIF565UC2G)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  METHYLPARABEN (UNII: A2I8C7HI9T)  EDETATE DISODIUM (UNII: 7FLD91C86K)  GLYCERIN (UNII: PDC6A3C0OX)  TROLAMINE (UNII: 9O3K93S3TK)  CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  OCTOXYNOL-9 (UNII: 7JPC6Y25QS)  DIPROPYLENE GLYCOL (UNII: E107L85C40)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0203-00 3.5 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 OTC monograph not final part348 09/19/2018 Part 3 of 8 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 PHOSPHATE, DIBASIC (UNII: GR686LBA74)  SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  SODIUM CHLORIDE (UNII: 451W47IQ8X)  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 final part349 12/18/2018 Part 4 of 8 TRIPLE ANTIBIOTICÂ
bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointmentProduct Information Item Code (Source) NDC:0498-0750 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 5000 [iU]  in 1 g BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 400 [iU]  in 1 g NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Product Characteristics Color white Score     Shape Size Flavor Imprint Code Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0750-35 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 OTC monograph final part333B 09/19/2018 Part 5 of 8 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 NDC:0498-0501-00 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 OTC monograph not final part333E 12/22/2017 Part 6 of 8 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 NDC:0498-0733-00 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 OTC monograph not final part348 12/23/2017 Part 7 of 8 HYDROCORTISONEÂ
anti-itch cream ointmentProduct Information Item Code (Source) NDC:0498-0800 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE ACETATE (UNII: 3X7931PO74) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE ACETATE 1 g  in 100 g Inactive Ingredients Ingredient Name Strength LIGHT MINERAL OIL (UNII: N6K5787QVP)  POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  CETYL ALCOHOL (UNII: 936JST6JCN)  METHYLPARABEN (UNII: A2I8C7HI9T)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  EDETATE DISODIUM (UNII: 7FLD91C86K)  STEARIC ACID (UNII: 4ELV7Z65AP)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  TROLAMINE (UNII: 9O3K93S3TK)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  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 OTC monograph not final part348 03/06/2013 10/15/2019 Part 8 of 8 PVP IODINE WIPEÂ
povidone-iodine 10% swabProduct Information Item Code (Source) NDC:0498-0121 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE 10 mg  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  NONOXYNOL-9 (UNII: 48Q180SH9T)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0121-00 0.3 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 09/18/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/13/2018 Labeler - Honeywell Safety Products USA, Inc. (118768815)