Label: 4234 FIRST AID KIT- 4234 first aid

  • NDC Code(s): 0498-0203-00, 0498-0501-00, 0498-0750-36, 0498-3334-00, view more
    0498-4234-01, 59898-403-10
  • 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 March 27, 2019

If you are a consumer or patient please visit this version.

  • Active ingredient

    Ammonia 15%

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  • Purpose

    Respiratory stimulant

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  • Uses

    to prevent or treat fainting

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  • Warnings

    For external use only

    Do not use

    • if you have asthma or emphysema

    Stop use and ask a doctor if

    • condition persists
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  • Keep out of reach of children

    If swallowed get medical help or contact a Poison Control Center right away.

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  • Directions

    • hold inhalant away from face and crush ampoule between thumb and forefinger at position indicated on sleeve.
    • hold near nostrils for inhalation of volatile vapor
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  • Other information

    store at room temperature away from light

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  • Inactive ingredients

    alcohol USP, FD&C red #40, lavender oil, lemon oil fcc, nutmeg oil, purified water

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  • Questions or Comments

    1-800-430-5490

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  • Burn Jel Active ingredient

    Lidocaine HCl 2.0%

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  • Burn Jel Purpose

    External analgesic

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  • Burn Jel Uses

    • temporarily relieves pain due to minor burns
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  • Burn Jel Warnings

    For external use only

    Do not use

    • on large areas of the body, particularly over raw surfaces or blistered areas

    When using this product

    • avoid contact with eyes

    Stop use and ask a doctor if

    • the condition gets worse
    • symptoms persist for more than 7 days
    • condition clears up and recurs within a few days

    Keep out of reach of children

    • If swallowed, get medical help or contact a Poison Control Center right away.
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  • Burn JEl Directions

    • adults and children 2 years of age and older; apply to affected area not more than 3 to 4 times daily
    • children under 2 years of age: ask a doctor
    • you may report a serious reaction to this product to 800-430-5490
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  • Burn Jel Other information

    • store at room temperature - do not use if opened or torn
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  • Burn Jel Inactive ingredients

    carbopol 940, carbopol 1342, diazolidinyl urea, glycerin, melaleuca alternifolia (tea tree) leaf oil, methylparaben, octoxynol-9, propylene glycol, propylparaben, trolamine, water

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  • Burn Jel Questions

    1-800-430-5490

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  • Triple Active ingredient

    Bacitracin zinc 400 units

    Neomycin sulfate (5 mg equivalent to 3.5 mg Neomycin base)

    Polymyxin B sulfate 5000 units

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  • Triple Purpose

    First aid antibiotic

    First aid antibiotic

    First aid antibiotic

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  • Triple Uses


    first aid to help prevent infection in:

    • minor cuts
    • scrapes
    • burns
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  • 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


    Stop use and ask a doctor if

    • the condition persists or gets worse
    • a rash or other allergic reaction develops
    • you need to use longer than 1 week


    Keep out of the reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.

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  • Triple Directions

    • clean the affected area
    • apply a small amount of the product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily
    • may be covered with a sterile bandage
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  • Triple Other information

    • store at 15 0 to 25 0 C (59 0 to 77 0 F)
    • tamper evident sealed packets
    • do not use if packet is torn or opened
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  • Triple Inactive ingredient

    petrolatum

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  • Triple Questions?

    1-800-430-5490

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  • BZK Wipe Active ingredient

    Benzalkonium chloride 0.13% w/v

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  • BZK Wipe Purpose

    First aid antiseptic

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  • BzK Wipe Uses

    Antiseptic cleansing of face, hands, and body without soap and water

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  • BZK Wipe Warnings


    For external use only

    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


    Stop use and ask a doctor if

    • if irritation, redness or other symptoms develop
    • the condition persists or gets worse

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.

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  • BZK Wipe Directions

    tear open packet and use as a washcloth

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  • BZK Wipe Other information

    • store at room temperature 15 0 to 30 0 C (59 0 - 86 0 F)
    • do not reuse towelette
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  • BZK Wipe Other information

    water

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  • BZK Wipe Questions

    1-800-430-5490

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  • Hydrogen Peroxide Active ingredient

    Hydrogen peroxide 3%

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  • Hydrogen Peroxide Purpose

    First aid antiseptic

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  • Hydrogen peroxide Uses

    • first aid to help prevent infection in minor cuts, scrapes and burns
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  • Hydrogen peroxide Warnings

    For external use only

    Do not use

    • in the eyes or apply over large areas of the body
    • longer than 1 week unless directed by a doctor

    Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • or serious burns

    Stop use and ask a doctor if

    • the condition persists or gets worse

    Keep out of reach of children


    If swallowed, get medical help or contact a Poison Control Center right away.

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  • Hydrogen peroxide Directions

    • clean the affected area
    • spray a small amount of this product on the area 1 to 3 times daily
    • may be covered with a sterile bandage
    • if bandaged, let dry first
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  • Hydrogen peroxide Other information

    • store at room temperature
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  • Hydrogen peroxide Inactive ingredient

    purified water

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  • Hydrogen peroxide Questions or Comments?

    1-800-430-5490

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  • 4234 68180SIGMA Kit Contents

    1 WOVEN 7/8 X 3 50/BOX

    1 FNGERTP LRG WOVEN 25/BOX

    1 FNGERTP WOVEN REG 40/BOX

    1 WOVEN 2" X 3" 25/BOX

    1 SWIFT KNUCKLE 40/BX

    1 AMMONIA INHALANTS 10 PER

    1 EYE DRESS PKT W/4 ADH STRIPS

    1 BURN JEL 1/8 OZ, 6 PER

    1 NITRILE GLOVES 2PR BBP

    1 ADHESIVE TAPE W/P 1/2"X 5 YD

    1 HYDROGEN PEROXIDE SPRAY PUMP

    1 GAUZE BANDAGE 4"X2 YDS STRETCH GZ

    1 FIRST AID GUIDE ASHI

    2 BLOODSTOPPER

    1 NON ADHERENT PADS 2"X3" 50'S

    1 COTTON BALLS STERILE 130

    1 ANTISEPTIC WIPES BZK CHL 20'S

    1 TRIPLE BIOTIC .5 GRAM PKT 20

    2 COLD PACK 5"X9" BOXED

    1 SCISSOR BDGE 4" RED PLS HDL

    1 KIT TWEEZER 3 1/2" SLANTED

    1 180 EMPTY BLANK NO LOGO

    1 BANDAGE COMP 3" W/TELFA PAD 2

    LBL STOCK 6-3/8"X4"

    1 LBL STOCK 4"X2-7/8"

    1 LBL STOCK 3"x1-7/8"

    1 TRI BNDG NON WOVEN 40"X40"X56"

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  • Principal Display Panel
  • Burn Jel Principal Display Panel
  • Triple Principal Display Panel
  • BZK Wipe Principal Display Panel
  • Hydrogen peroxide Principal Display Panel
  • 4234 Kit Label 68180SIGMA
  • INGREDIENTS AND APPEARANCE
    4234 FIRST AID KIT 
    4234 first aid kit
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4234
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-4234-01 1 in 1 KIT 09/13/2018
    Quantity of Parts
    Part # Package Quantity Total Product Quantity
    Part 1 1 BOTTLE, SPRAY 59 mL
    Part 2 10 AMPULE 3 mL
    Part 3 6 PACKET 21 g
    Part 4 20 PACKET 10 g
    Part 5 20 PACKET 28 mL
    Part 1 of 5
    WATER JEL HYDROGEN PEROXIDE 
    hydrogen peroxide spray
    Product Information
    Item Code (Source) NDC:59898-403
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE 3 mL  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:59898-403-10 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
    OTC monograph not final part333A 05/01/2013
    Part 2 of 5
    AMMONIA INHALENT 
    ammonia inhalent inhalant
    Product 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
    Part 3 of 5
    BURN JEL 
    gel for burns gel
    Product 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 4 of 5
    TRIPLE ANTIBIOTIC 
    bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointment
    Product 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:0498-0750-36 0.5 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 final part333B 09/19/2018
    Part 5 of 5
    ANTISEPTIC TOWELETTE 
    benzalkonium chloride liquid
    Product 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
    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. (079287321)
    Registrant - Honeywell Safety Products USA, Inc. (079287321)
    Establishment
    Name Address ID/FEI Business Operations
    James Alexander 040756421 manufacture(0498-3334)
    Establishment
    Name Address ID/FEI Business Operations
    Honeywell Safety Products USA, Inc 079287321 pack(0498-4234)
    Establishment
    Name Address ID/FEI Business Operations
    Water-Jel Technologies 155522589 manufacture(0498-0203, 0498-0750, 59898-403)
    Establishment
    Name Address ID/FEI Business Operations
    Changzhou Maokang Medical 421317073 manufacture(0498-0501)
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