Label: WET WIPE- benzalkonium chloride swab

  • NDC Code(s): 76906-002-01, 76906-002-02, 76906-002-04, 76906-002-05, view more
    76906-002-06, 76906-002-07, 76906-002-08, 76906-002-09, 76906-002-10, 76906-002-11, 76906-002-12
  • Packager: Yiwu Beitao Infant & Mother Supplies Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated July 15, 2020

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  • Active Ingredient

    Benzalkonium Chloride 0.13%

    Purpose

    Antimicrobial

  • USE

    For hand washing to decrease bacteria on the skin.
    Recommended for repeated use.

  • Warning

    For external use only
    When using this product, avoid contact with the eyes.
    In case of contact, flush eyes thoroughly with water.
    Stop use and ask a doctor if irritation and redness develop.

    Keep out of reach of children. If swallowed, get medical help
    or contact a Poison Control Center right away.

  • Directions

    For hand sanitizing to decrease bacteria on the skin.
    Recommended for repeated use.

  • Inactive ingredients

    Aqua, Propylene Glycol, Polysorbate 20, Phenoxyethanol.

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    WET WIPE 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76906-002
    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)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76906-002-07100 in 1 BOX03/21/2020
    14.8 g in 1 POUCH; Type 0: Not a Combination Product
    2NDC:76906-002-08135 in 1 PAIL03/21/2020
    22.07 g in 1 POUCH; Type 0: Not a Combination Product
    3NDC:76906-002-0110 in 1 BAG03/21/2020
    35 g in 1 POUCH; Type 0: Not a Combination Product
    4NDC:76906-002-0450 in 1 BAG03/21/2020
    46 g in 1 POUCH; Type 0: Not a Combination Product
    5NDC:76906-002-0220 in 1 BAG03/21/2020
    56.5 g in 1 POUCH; Type 0: Not a Combination Product
    6NDC:76906-002-05350 in 1 BAG03/21/2020
    65.8 g in 1 POUCH; Type 0: Not a Combination Product
    7NDC:76906-002-0680 in 1 BAG03/21/2020
    75.25 g in 1 POUCH; Type 0: Not a Combination Product
    8NDC:76906-002-09250 in 1 PAIL03/21/2020
    82.08 g in 1 POUCH; Type 0: Not a Combination Product
    9NDC:76906-002-1060 in 1 PAIL03/21/2020
    95.83 g in 1 POUCH; Type 0: Not a Combination Product
    10NDC:76906-002-1125 in 1 BAG03/21/2020
    108 g in 1 POUCH; Type 0: Not a Combination Product
    11NDC:76906-002-12100 in 1 BAG03/21/2020
    114.8 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/21/2020
    Labeler - Yiwu Beitao Infant & Mother Supplies Co., Ltd. (412925352)
    Establishment
    NameAddressID/FEIBusiness Operations
    Yiwu Beitao Infant & Mother Supplies Co., Ltd.412925352manufacture(76906-002)
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