Label: 4237 FIRST AID KIT kit

  • NDC Code(s): 0498-0121-00, 0498-0143-04, 0498-0202-00, 0498-4237-01
  • 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 26, 2021

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

  • Burn Jel Active ingredient

    Lidocaine HCl 2.0%

  • Burn Jel Purpose

    External analgesic

  • Burn Jel Uses

    temporarily relieves pain due to minor burns

  • 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
  • Burn Jel Keep out of reach of children

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

  • 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
  • Burn Jel Other information

    • store at room temperature
    • do not use if opened or torn
  • 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

  • Burn Jel Questions

    1-800-430-5490

  • PVP Wipe Active ingredient

    Povidone-iodine 10%

    (equivalent to 1% titratable iodine)

  • PVP Wipe Purpose

    First aid antiseptic

  • PVP Wipe Uses

    first aid antiseptic to help prevent infection in minor cuts, scrapes and burns

  • PVP Wipe 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

  • PVP Wipe Keep out of reach of children

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

  • PVP Wipe 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
  • PVP Wipe 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
  • PVP Wipe Inactive ingredients

    nonoxynol 9, water

  • PVP Wipe Questions

    800-430-5490

  • Alcohol Active ingredient

    Isopropyl alcohol 70%

  • Alcohol Purpose

    First aid antiseptic

  • Alcohol Uses

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

    For external use only

    Flammable, keep away from fire and flame

    Do not use

    • in or near eyes
    • over large areas of the body

    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

  • 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
  • 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
  • Alcohol Inactive ingredient

    water

  • Alcohol Questions

    1-800-430-5490

  • 4237 6836ALPD3 Kit Contents

    1 GAUZE BANDAGE, 2" X 6 YD,2 PER

    2 INSTANT COLD PACK 4" X 6"

    1 EYEWASH BOTTLES 1 OZ, UNITIZED 2/BX

    1 BURN JEL 1/8 OZ, 6 PER

    1 WATER JEL DRESSING 4" X 4"

    1 ALCOHOL PREP PADS 10P

    4 ADH BDG, CLOTH, 1"X3", 16 PER

    1 FIRST AID GUIDE ASHI

    1 SCISSOR UTILITY SHEARS 7-1/4"

    1 ISO-SHIELD CPR ADULT/CHLD 1BG

    LBL STOCK 6-3/8"X4"

    1 LBL STOCK 6-3/8"X4"

    LBL STOCK 4"X2-7/8"

    1 LBL STOCK 3"x1-7/8"

    1 PICK-UP SCOOP W/SCRAPER

    1 WATER-JEL BURN DRESSING 2 X 6

    1 KIT STL 36 UN WHT 01 HOR SHELF

    1 KNUCKLE BANDS 16'S

    1 ADHS TAPE .5"X2.5YD 2

    1 FINGERTIP "T" 8/BX

    1 PVP IODINE SWABS 10

    1 GAUZE PADS 3"X3" 4/BX

    1 SCISSOR & FORCEP 1 EA

    1 RESCUE BLANKET 1EA

    1 RED BIO BAGS 2/BX

    1 FACE MASK/EYE SHIELD

    1 LIQD TRTMNT SYS 1 EA

    1 DISP. TOWEL/WIPES 2EA

    3 NITRILE GLOVES 1 PR

  • Burn Jel Principal Display Panel

    Burn Jel

  • PVP Wipe Principal Display Panel

    PVP wipes

  • Alcohol Principal Display Panel

    Alcohol Preps

  • 4237 Kit Label 6836ALPD3

    4237 label

  • INGREDIENTS AND APPEARANCE
    4237 FIRST AID KIT 
    4237 first aid kit kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0498-4237
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0498-4237-011 in 1 KIT09/12/2018
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 16 PACKET 21 mL
    Part 220 POUCH 6 mL
    Part 310 POUCH 4 mL
    Part 1 of 3
    BURN JEL 
    gel for burns gel
    Product Information
    Item Code (Source)NDC:0498-0202
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    OCTOXYNOL 9 (UNII: 7JPC6Y25QS)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31)  
    CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0498-0202-003.5 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34812/08/2017
    Part 2 of 3
    PVP IODINE WIPE 
    povidone-iodine 10% swab
    Product Information
    Item Code (Source)NDC:0498-0121
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    NONOXYNOL-9 (UNII: 48Q180SH9T)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0498-0121-000.3 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/18/2018
    Part 3 of 3
    ALCOHOL WIPE 
    isopropyl alcohol swab
    Product Information
    Item Code (Source)NDC:0498-0143
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0498-0143-040.4 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/18/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/12/2018
    Labeler - Honeywell Safety Products USA, Inc. (079287321)