CVS PET WOUND CARE PREP-PACK (BENZALKONIUM CHLORIDE) KIT [CVS]

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CVS PET WOUND CARE PREP-PACK (BENZALKONIUM CHLORIDE) KIT [CVS]
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NDC 52124-0001-1, 69842-405-00
Set ID 44aa37e6-e6a8-022a-e054-00144ff88e88
Category HUMAN OTC DRUG LABEL
Packager CVS
Generic Name
Product Class
Product Number
Application Number PART333A
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  • Active Ingredient

    Benzalkonium Chloride .13%

  • Purpose

    First Aid Antiseptic

  • Use

    For Professional and Hospital use. Helps prevent infection. Antiseptic cleansing of face, hands and body without soap and water.

  • Warnings

    For external use only. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. If unusual redness, swelling or other symptoms occur, cunsult a physician immediately.

  • KEEP OUT OF REACH OF CHILDREN

  • STOP USE

  • Do not use

    In the eyes, or over large areas of the body

  • Directions

    Tear open packet, unfold towelette and use to cleanse desired skin are. Discard towelette appropriately after single use

  • Inactive Ingredients

    Purified Water

  • Antiseptic Towelette

    Pet Wound Care Prep-PackAntiseptic Towelette
    GFA Production Xiamen Co., Ltd
    www.gfaproduction.com

    Antiseptic Towelette

  • INGREDIENTS AND APPEARANCE
    CVS PET WOUND CARE PREP-PACK 
    benzalkonium chloride kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-405
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69842-405-001 in 1 BAG; Type 0: Not a Combination Product12/01/2016
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 18 PACKAGE 6 mL  in .8 
    Part 1 of 1
    ANTISEPTIC 
    benzalkonium chloride swab
    Product Information
    Item Code (Source)NDC:52124-0001
    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:52124-0001-10.8 mL in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E12/01/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333A12/01/2016
    Labeler - CVS (062312574)
    Establishment
    NameAddressID/FEIBusiness Operations
    Tender Corporation064437304manufacture(69842-405)
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