Label: 4267 FIRST AID KIT kit
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NDC Code(s):
0498-0100-02,
0498-0143-04,
0498-0221-59,
0498-0402-59, view more0498-0730-01, 0498-3334-00, 0498-4267-01, 59898-420-36
- 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)
- Eyesaline Active ingredient
- Eyesaline Purpose
- Eyesaline Uses
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Eyesaline
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.
- Eyesaline Directions
- Eyesaline Inactive ingredients
- Eyesaline Questions
- Alcohol Wipe Active ingredient
- Alcohol Wipe Purpose
- Alcohol Wipe Uses
- Alcohol Wipe Warnings
- Alcohol Wipe Directions
- Alcohol Wipe Other information
- Alcohol Wipe Inactive ingredient
- Alcohol Wipe Questions
- Aypanal Active ingredient
- Aypanal Purpose
- Aypanaly Uses
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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 more than 5 doses in 24 hours, which is the maximum daily amount
- taken with other drugs containing acetaminophen
- adult has 3 or more alcoholic drinks every day while using this product:
Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:
- skin reddening
- blisters
- rash
- If a skin rash occurs, stop use and seek medical help right away.
Do not use
- with any other drug containing acetaminophen (prescription or nonprescription).
- If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
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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 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
- Neomycin Active ingredient
- Neomycin Purpose
- Neomycin Uses
- Neomycin Warnings
- Neomycin Direction
- Neomycin Other information
- Neomycin Inactive ingredient
- Neomycin Questions?
- Antiseptic Spray Active ingredient
- Antiseptic Spray Purpose
- Antiseptic Spray Uses
- Antiseptic Spray Warnings
- Antiseptic Spray Directions
- Antiseptic Spray Other information
- Antiseptic Spray Inactive ingredients
- Antiseptic Spray Questions
- Burn Spray Active ingredient
- Burn Spray Purpose
- Burn Spray Uses
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Burn Spray
Warnings
For external use only
Flammable
- keep away from fire or flame
- contents under pressure
- do not puncture or incinerate container
- do not expose to temperatures above 120 0 F
Do not use
- in or near the eyes or other mucous membranes
- in case of serious burns
- in case of deep or puncture wounds
- for prolonged period of time
- on large portion of the body
- Burn Spray Directions
- Burn Spray Other information
- Burn Spray Inactive ingredients
- Hand Sanitizer Active ingredient
- Hand Santizer Purpose
- Hand Sanitizer Uses
- Hand Sanitizer Warnings
- Hand Sanitizer Directions
- Hand Sanitizer Other information
- Hand Sanitizer Inactive ingredients
- Hand Sanitizer Questions or Comments?
- Ammonia Active ingredient
- Ammonia Purpose
- Ammonia Uses
- Ammonia Warnings
- Ammonia Directions
- Ammonia Other information
- Ammonia Inactive ingredients
- Ammonia Questions or Comments?
- Eyesaline Principal Display Panel
- Alcohol Wipe Principal Display Panel
- Aypanal Principal Display Panel
- Neomycin Principal Display Panel
- Antiseptic Spray Principal Display Panel
- Burn Spray Principal Display Panel
- Hand Sanitizer Principal Display Panel
- Ammonia Principal Display Panel
- 4267 Kit Label FAK3SHLF-CLSB
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4267 Kit Contnets
FAK3SHLF-CLSB
1 1X3 PLASTIC 100/BOX
1 FINGERTIP "T" WOVEN 40/BOX
1 SWIFT KNUCKLE 40/BX
1 1 X 3 WOVEN 100/BOX
3 NEOMYCIN ANTIBIOTIC 10 PER
1 AMMONIA INHALANTS 10 PER
2 EYE DRESS PKT W/4 ADH STRIPS
1 TOURNIQUET, 1 PER
1 WIRE SPLINT 1 PER
1 ADH BAND, EXTRA LARGE, 6 PER
1 ALCOHOL PREP PADS 10P
1 O/H PUMP ANTISEPTIC 2 OZ ID F
1 O/H PUMP BURN RELIEF 2 OZ ID G
1 FIRST AID GUIDE ASHI
2 TAPE ADHESIVE 1"X 5 YD PLSTC
10 HAND SANITIZER 0.9G WJ BULK
4 GAUZE CLEAN-WRAP BDGE N/S 2"
4 GAUZE CLEAN-WRAP BDGE N/S 4"
4 BLOODSTOPPER
1 NON-ADHERENT PADS 2"X3" 10'S
1 GZE PADS STERILE 2"X 2" 10'S
1 GZE PADS STERILE 3"X 3" 25'S
1 ELASTIC BANDAGE 3" X 4.5YD
1 CPR FILTERSHIELD 77-100
1 COTTON TIPS 100 PER VIAL
1 AYPANAL NON-ASP IND 2/ENV 100
1 4OZ BFS EYEWASH TRILINGUAL BOTTLE
1 SCISSOR BDGE 4" RED PLS HDL
1 KIT TWEEZER 3 1/2" SLANTED
1 180 EMPTY BLANK NO LOGO
1 POCKET INSERT RED #180 KIT 4R
1 TONGUE BLADES SR WRAPPED 6'S
1 LBL STOCK 6-3/8"X4"
1 LBL STOCK 4"X2-7/8"
1 LBL STOCK 3"x1-7/8"
4 PR LRG NITRILE GLVES ZIP BAG
2 WATER-JEL BURN DRESSING 4 X 4
1 LBL CONTENTS ANSI 2015 CL B
1 LBL CAB CVR ANSI 2015 CL B
2 TRI BNDG NON WOVEN 40"X40"X56"
2 COLD PACK UNIT 4"X6" BULK
1 RED BIO BAGS 2/BX
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INGREDIENTS AND APPEARANCE
4267 FIRST AID KITÂ
4267 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4267 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4267-01 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 118 mL Part 2 10 POUCH 4 mL Part 3 50 PACKET 100 Part 4 1 BOTTLE, SPRAY 59 mL Part 5 1 BOTTLE, SPRAY 59 mL Part 6 30 PACKET 27 g Part 7 10 PACKAGE 9 mL Part 8 10 AMPULE 3 mL Part 1 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 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:0498-0100-02 118 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 8 ALCOHOL WIPEÂ
isopropyl alcohol swabProduct Information Item Code (Source) NDC:0498-0143 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 0.7 mL  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0143-04 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 09/18/2018 Part 3 of 8 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 STARCH, CORN (UNII: O8232NY3SJ)  STEARIC ACID (UNII: 4ELV7Z65AP)  POVIDONE (UNII: FZ989GH94E)  SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  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 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 4 of 8 BURN RELIEFÂ
lidocaine hydrochloride sprayProduct Information Item Code (Source) NDC:0498-0221 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 24.64 mg  in 1 mL Inactive Ingredients Ingredient Name Strength EDETATE DISODIUM (UNII: 7FLD91C86K)  GLYCERIN (UNII: PDC6A3C0OX)  TROLAMINE (UNII: 9O3K93S3TK)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  WATER (UNII: 059QF0KO0R)  OCTOXYNOL-9 (UNII: 7JPC6Y25QS)  HYPROMELLOSES (UNII: 3NXW29V3WO)  TEA TREE OIL (UNII: VIF565UC2G)  METHYLPARABEN (UNII: A2I8C7HI9T)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0221-59 59 mL in 1 BOTTLE, SPRAY; 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 Part 5 of 8 ANTISEPTICÂ
benzalkonium chloride sprayProduct Information Item Code (Source) NDC:0498-0402 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 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  OCTOXYNOL 9 (UNII: 7JPC6Y25QS)  GLYCERIN (UNII: PDC6A3C0OX)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  DIPROPYLENE GLYCOL (UNII: E107L85C40)  EDETATE DISODIUM (UNII: 7FLD91C86K)  TROLAMINE (UNII: 9O3K93S3TK)  METHYLPARABEN (UNII: A2I8C7HI9T)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0402-59 59 mL in 1 BOTTLE, SPRAY; 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 Part 6 of 8 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 7 of 8 INSTANT HAND SANITIZERÂ
alcohol liquidProduct Information Item Code (Source) NDC:59898-420 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL  in 100 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)  WATER (UNII: 059QF0KO0R)  TRIISOPROPANOLAMINE (UNII: W9EN9DLM98)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59898-420-36 0.9 mL in 1 PACKAGE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/15/2010 Part 8 of 8 AMMONIA INHALENTÂ
ammonia inhalent inhalantProduct Information Item Code (Source) NDC:0498-3334 Route of Administration RESPIRATORY (INHALATION) Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) AMMONIA 0.045 g  in 0.3 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-3334-00 0.3 mL in 1 AMPULE; 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 12/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 Labeler - Honeywell Safety Products USA, INC (118768815)