Label: 4129 FIRST AID KIT- 4129 first aid kit

  • NDC Code(s): 0498-0011-77, 0498-0121-00, 0498-0143-04, 0498-0501-00, view more
    0498-0733-00, 0498-0800-34, 0498-3334-00, 0498-4129-01
  • 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 October 16, 2019

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

  • Ammonia Active ingredient

    Ammonia 15%

    Close
  • Ammonia Purpose

    Respiratory stimulant

    Close
  • Ammonia Uses

    • to prevent or treat fainting
    Close
  • Ammonia Warnings

    For external use only

    Do not use

    • if you have breathing problems such as asthma or emphysema

    Stop use and ask a doctor if

    • condition persists

    Keep out of reach of children

    • If swallowed get medical help or contact a Poison Control Center right away.
    Close
  • Ammonia 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
    Close
  • Ammonia Other information

    • store at room temperature away from light
    Close
  • Ammonia Inactive ingredient

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

    Close
  • Ammonia Questions or Comments?

    1-800-430-5490

    Close
  • Pyrocaine Active ingredient

    Benzocaine 20%

    Benzethonium chloride 0.2%

    Close
  • Pyrocaine Purpose

    Topical anesthetic

    Topical antiseptic

    Close
  • Pyrocaine Uses

    For the temporary relief of pain and itching, and to help protect against skin infection in:

    • minor burns
    • minor skin irritations
    • minor cuts and scrapes
    • insect bites
    • sunburns

    Do not use

    • in or near the eyes or over large portions of the body
    • in case of deep or puncture wounds or on:
    • raw surfaces
    • blistered areas
    • animal bites
    • serious burns

    Keep out of reach of children

    • If swallowed, get medical help or contact a Poison Control Center right away
    Close
  • Pyrocaine Warnings

    For external use only

    Flammable

    • keep away from fire or flame
    • contents under pressure
    • do not puncture, incinerate or expose container to temperatures above 120 o F

    Stop use and ask a doctor if

    • If condition persists or worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days
    Close
  • Pyrocaine Directions

    • clean the affected area
    • shake can well before using
    • hold can 6 to 12 inches away from the affected area and spray liberally
    • apply to affected area not more than 3 times daily
    • for adult institutional use only
    • not intended for use on children
    Close
  • Pyrocaine Other information

    • avoid inhaling
    • use only as directed
    • intentional misuse by deliberately concentrating and inhaling the contents may be harmful or fatal
    Close
  • Pyrocaine Inactive ingredients


    butane,dipropylene glycol, isobutane, propane

    Close
  • PVP Active ingredient

    Povidone-iodine 10%

    (equivalent to 1% titratable iodine)

    Close
  • PVP Purpose

    First aid antiseptic

    Close
  • PVP Uses

    • first aid antiseptic to help prevent infection in minor cuts, scrapes and burns
    Close
  • PVP Warnings

    For external use only.

    Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • serious burns

    Stop use and ask a doctor if

    • condition worsens or persists for more than 72 hours
    • irritation and redness develops

    Keep out of reach of children.

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

    Close
  • PVP Directions

    • clean the affected area
    • apply1 to 3 times daily
    • may be covered with a sterile bandage
    • if bandaged, let dry first
    • discard wipe after single use
    Close
  • PVP Other information

    • do not use on individuals who are allergic or sensitive to iodine
    • store at controlled temperature 59-86ºF (15-30ºC)
    • do not use if pouch is open or torn
    Close
  • PVP Inactive ingredients

    nonoxynol 9, water

    Close
  • PVP Questions

    1-800-430-5490

    Close
  • Sting Relief Active ingredient (in each wipe)

    Ethyl alcohol 50.0%

    Lidocaine HCl 2.0%

    Close
  • Sting Relief Purpose

    Antiseptic

    Topical pain relief

    Close
  • Sting Relef Uses

    • prevent infection in minor scrapes, and temporary relief of itching of insect bites
    Close
  • Sting Relief Warnings

    For external use only

    Flammable, keep away from open fire or flame

    Do not use

    • over large areas of the body
    • in eyes
    • over raw or blistered areas

    Stop use and ask a doctor

    • if conditions worsen or persist for more than 7 days or clear up and occur again within a few days

    Keep out of reach of children.

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

    Close
  • Sting Relief Directions

    • adults and children 2 years and older: Apply to cleaned affected area not more than 3 times daily.
    • children under 2 years of age: consult a doctor.
    Close
  • Sting Relief Inactive ingredients

    benzalkonium chloride, menthol, and purified water

    Close
  • Sting Relief Questions or Comments?

    1-800-430-5490

    Close
  • alcohol Active ingredient

    Isopropyl alcohol 70%

    Close
  • Alcohol Purpose

    First aid antiseptic

    Close
  • Alcohol Uses

    • first aid to help prevent infection in minor cuts, scrapes, and burnsv
    Close
  • Alcohol Warnings

    For external use only

    Flammable, keep away from fire and flame

    Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • serious burns

    When using this product

    • do not use longer than 1 week unless directed by a doctor

    Stop use and consult a doctor if

    • condition persists or gets worse

    Keep out of the reach of children

    • If swallowed, get medical help or contact a Poison Control center right away
    Close
  • Alcohol Directions

    • clean the affected area
    • may be covered with a sterile bandage
    • apply wipe to affeted are 1 to 3 times daily
    • discard wipe after single use
    Close
  • Alcohol Other information

    • store at room temperature 15 0 to 25 0 C (59 0 to 77 0 F)
    • do not use if packet is torn or opened
    Close
  • Alcohol Inactive ingredient

    water

    Close
  • Alcojol Questions

    1-800-430-5490

    Close
  • Hydrocortisone Active ingredient (in each gram)

    Hydrocortisone acetate (equivalent to Hydrocortisone 1%)

    Close
  • Hydrocortisone Purpose

    Anti-itch cream

    Close
  • Hydrocortisone Uses

    • for the temporary relief of itching associated with minor skin irritations and rashes
    Close
  • Hydrocortisone Warnings

    For external use only

    Ask a doctor before use

    • if you are using any other hydrocortisone product

    When 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

    Stop use and ask a doctor if

    • condition worsens
    • condition persists 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.

    Close
  • Hydrocortisone Directions

    • adults and children 2 years and older:
    • clean the affected area
    • apply to the area not more than 3 to 4 times daily
    • children under 2 years of age: consult a doctor
    Close
  • Hydrocortisone Other information

    • store at room temperature (do not freeze)
    Close
  • Hydrocortisone Inactive ingredients

    cetyl alcohol, citric acid, diazolidinyl urea, edetate disodium, glycerin, glyceryl monostearate, methylparaben, mineral oil, polyethylene glycol, propylene glycol, propylparaben, purified water, stearic acid, trolamine

    Close
  • Hydrocortisone Questions or comments?

    1-800-430-5490

    Close
  • BZK Active ingredient

    Benzalkonium chloride 0.13% w/v

    Close
  • BZK Purpose


    First aid antiseptic

    Close
  • BZK Uses

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

    Close
  • BZK 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.

    Close
  • BZK Directions

    • tear open packet and use as a washcloth
    Close
  • BZK Other information

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

    Close
  • BZK Inactive ingredient

    water

    Close
  • BZK Questions

    1-800-430-5490

    Close
  • 4129 SF00004226 Kit Contents

    1 AMMONIA INHALANTS 10 PER

    1 EYE DRESS PKT W/4 ADH STRIPS

    1 TRIANGULAR BDG, NON-STERILE

    1 INSTANT COLD PACK 4" X 6"

    1 ALCOHOL PREP PADS 10P

    1 HYDROCORTISON,1.O%,1/32 OZ,10P

    1 RESPONSE KIT BLOODBORNE PATHOG

    1 SCISSOR BDGE 4" RED PLS HDL

    1 BANDAGE COMP 2" W/TELFA PAD 4

    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"

    1 PR LRG NITRILE GLVES ZIP BAG

    1 1" X 3" PLASTIC BANDS 16/BAG

    1 KIT STL 24 UN WHITE 01

    1 PVP IODINE SWABS 10

    1 STING Relief SWAB 10

    1 PYRO-CAINE AERO 2/BX

    1 RED BIO BAGS 2/BX

    1 FACE MASK/EYE SHIELD

    1 LIQD TRTMNT SYS 1 EA

    1 DISP. TOWEL/WIPES 2EA

    1 IMPERVIOUS GOWN 1 EA

    Close
  • Ammonia Principal Display Panel
  • Pyrocaine Principal Display Panel
  • PVP Principal Display Panel
  • Sting Relief Principal Display Panel
  • Alcohol Principal Display Panel
  • Hydrocortisone Principal Display Panel
  • BZK Principal Display Panel
  • 4129 Kit Label SF00004226
  • INGREDIENTS AND APPEARANCE
    4129 FIRST AID KIT 
    4129 first aid kit kit
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4129
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-4129-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018
    Quantity of Parts
    Part # Package Quantity Total Product Quantity
    Part 1 10 PACKET 9 g
    Part 2 10 AMPULE 3 mL
    Part 3 2 CAN 28.4 g
    Part 4 10 POUCH 4 mL
    Part 5 10 POUCH 3 mL
    Part 6 4 PACKET 5.6 mL
    Part 7 10 POUCH 4 mL
    Part 8 10 PACKET 9 g
    Part 1 of 8
    HYDROCORTISONE 
    anti-itch cream
    Product 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)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    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
    Part 2 of 8
    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 8
    PYROCAINE BURN 
    benzocaine, benzethonium chloride aerosol, spray
    Product Information
    Item Code (Source) NDC:0498-0011
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 20 g  in 100 g
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 0.2 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    1,1,3-TRI(3-TERT-BUTYL-4-HYDROXY-6-METHYLPHENYL)BUTANE (UNII: BF6E9O0XJN)  
    ISOBUTANE (UNII: BXR49TP611)  
    1,1,3-TRIS(2-CHLOROETHOXY)PROPANE (UNII: 4FEX9N888E)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-0011-77 14.2 g in 1 CAN; 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 01/01/2018
    Part 4 of 8
    STING RELIEF PAD 
    ethyl alcohol, lidocaine swab
    Product Information
    Item Code (Source) NDC:0498-0733
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    MENTHOL (UNII: L7T10EIP3A)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    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 5 of 8
    PVP IODINE WIPE 
    povidone-iodine 10% swab
    Product 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
    NONOXYNOL-9 (UNII: 48Q180SH9T)  
    WATER (UNII: 059QF0KO0R)  
    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
    Part 6 of 8
    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 12/21/2017
    Part 7 of 8
    ALCOHOL WIPE 
    isopropyl alcohol swab
    Product 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
    OTC monograph not final part333A 09/18/2018
    Part 8 of 8
    HYDROCORTISONE 
    anti-itch cream ointment
    Product 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)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-0800-34 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
    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 (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(0498-4129)
    Establishment
    Name Address ID/FEI Business Operations
    Dixon Investments 115315822 manufacture(0498-0011)
    Establishment
    Name Address ID/FEI Business Operations
    Water-Jel Technologies 155522589 manufacture(0498-0800, 0498-0801)
    Establishment
    Name Address ID/FEI Business Operations
    Chanzhou Maokang Medical 421317073 manufacture(0498-0143, 0498-0501)
    Establishment
    Name Address ID/FEI Business Operations
    Sion Medical Biotext 532775194 manufacture(0498-0121)
    Establishment
    Name Address ID/FEI Business Operations
    Safetec of America Inc 874965262 manufacture(0498-0733)
    Close