Label: ANTI-BACTERIAL ALL PURPOSE WIPE- benzalkonium chloride cloth

  • NDC Code(s): 77720-024-01, 77720-024-02, 77720-024-03, 77720-024-04, view more
    77720-024-05, 77720-024-06, 77720-024-07
  • Packager: Skaffles Group Limited Liability Company
  • Category: OTC ANIMAL 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 January 22, 2021

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

  • Active Ingredient

    Benzalkonium Chloride 0.13%

    Purpose

    Antibacterial

  • USE

    Decreases Bacteria on pets body.

  • Warning

    For external use only.

    Avoid Contact with eyes. Safe for dogs 8 weeks of age and older.

    Keep out of reach of children.

  • Directions

    Remove wipe form canister&reseal to maintian freshness.

    wipe donw dog from back of neck to tail ,carefullly avoiding the eyes.

    didpose of wipe in trash ,do not flush

  • Inactive ingredients

    water,Aloe BarbadensisLeaf Juice, PEG-75 Lan olin,
    Quaternium-52, PEG-8 Dim ethicone, Fragran ce, DisodiumCocoamph odiacet ate, Disodium EDTA,Cham omilla Recutita(hMatricaria) FowerExtrad,Potassium Sorbate, Phenoxyeth an olCetylpyridinium Chloride, Sodium Benzoate, CitricAcid.

  • PRINCIPAL DISPLAY PANEL

    123

  • INGREDIENTS AND APPEARANCE
    ANTI-BACTERIAL ALL PURPOSE WIPE 
    benzalkonium chloride cloth
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:77720-024
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PEG-75 LANOLIN (UNII: 09179OX7TB)  
    QUATERNIUM-52 (UNII: 588EQF3H1P)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PEG-8 DIMETHICONE (UNII: GIA7T764OD)  
    DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
    DISODIUM EDTA-COPPER (UNII: 6V475AX06U)  
    CHAMOMILE (UNII: FGL3685T2X)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CITRIC ACID ACETATE (UNII: DSO12WL7AU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77720-024-0150 in 1 CANISTER
    1186 g in 1 NOT APPLICABLE
    2NDC:77720-024-0230 in 1 PACKAGE
    2112 g in 1 NOT APPLICABLE
    3NDC:77720-024-03100 in 1 PACKAGE
    3372 g in 1 NOT APPLICABLE
    4NDC:77720-024-0475 in 1 CANISTER
    4279 g in 1 NOT APPLICABLE
    5NDC:77720-024-0550 in 1 PACKAGE
    5186 g in 1 NOT APPLICABLE
    6NDC:77720-024-0675 in 1 POUCH
    6279 g in 1 NOT APPLICABLE
    7NDC:77720-024-07100 in 1 CANISTER
    7372 g in 1 NOT APPLICABLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/19/2021
    Labeler - Skaffles Group Limited Liability Company (831115642)
    Registrant - Skaffles Group Limited Liability Company (831115642)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Qimei Commodity Co.,Ltd.544331136manufacture
    Establishment
    NameAddressID/FEIBusiness Operations
    Lonza Guangzhou Nansha LTD545328150api manufacture