Label: 4268 FIRST AID KIT kit

  • NDC Code(s): 0498-0501-00, 0498-4268-01
  • Packager: Honeywell Safety Products USA, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Updated January 22, 2024

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  • Active ingredient

    Ethyl alcohol 66.5%

  • Purpose

    Antiseptic

  • Uses

    for handwashing to decrease bacteria on skin whenever soap and water is not readily available

  • Warnings

    For external use only


    Flammable: keep away from fire or flame

    Do not use

    • in the eyes. If this happens, rinse thoroughly with water.

    Stop use and ask a doctor if

    • irritation or redness develop and persists for more than 72 hours

    Keep out of reach of children


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

  • Directions

    • wet hands and wrists thoroughly for 15 seconds and allow to air dry
    • always reseal after use
    • children under 6 years of age should be supervised when using this product
  • Inactive ingredients

    aloe vera, fragrance, purified water, triethanolamine

  • Questions

    1-800-430-5490

  • BZK Active ingredient

    Benzalkonium chloride 0.13% w/v

  • BZK Purpose

    First aid antiseptic

  • BZK Uses

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

  • 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.

  • BZK Directions

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

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

    water

  • BZK Questions

    1-800-430-5490

  • 4268 SF00000669 Kit Contents

    3 PAWS PERS ANTIMICRO WIPE

    LBL STOCK 6-3/8"X4"

    LBL STOCK 3"x1-7/8"

    1 BZK ANTISEPTIC WIPE, BULK

    2 PR LRG NITRILE GLVES ZIP BAG

    1 FACEMASK W/SHLD EAR LOOP

    1 PICK-UP SCOOP W/SCRAPER

    1 SOLIDIFIER BBP POUCH 2 OZ ID E

    1 KIT, PP 10 UNIT FA

    2 BAG BIOHAZARD 24 X 24 RED

    2 TOWEL 3-FOLD WHITE

    2 TWIST TIE

  • PAWS Principal Display Panel

    PAWS

  • BZK Principal Display Panel

    Antiseptic Wipe

  • 4268 Kit Label SF00000669

    4268 label

  • INGREDIENTS AND APPEARANCE
    4268 FIRST AID KIT 
    4268 first aid kit kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0498-4268
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0498-4268-011 in 1 KIT10/13/2018
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 13 PACKET 0.0057 L
    Part 21 PACKET 1.4 mL
    Part 1 of 2
    ANTIMICROBIAL 
    alcohol liquid
    Product Information
    Item Code (Source)NDC:61010-3111
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL665 mL  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    ALOE (UNII: V5VD430YW9)  
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    110 in 1 BOX
    10.0019 L in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/21/2017
    Part 2 of 2
    ANTISEPTIC TOWELETTE 
    benzalkonium chloride liquid
    Product Information
    Item Code (Source)NDC:0498-0501
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0498-0501-001.4 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/21/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/13/2018
    Labeler - Honeywell Safety Products USA, Inc. (118768815)
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