Label: WET WIPE- alcohol swab

  • NDC Code(s): 76906-001-01, 76906-001-02, 76906-001-03, 76906-001-04, view more
    76906-001-05, 76906-001-06, 76906-001-07, 76906-001-08, 76906-001-09, 76906-001-13
  • Packager: Zhejiang BeiTao Hygienic Products Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated February 1, 2020

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  • Active Ingredient

    Ethanol 70%

    Purpose

    Antiseptice Handwash

  • USE

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

  • Warning

    For external use only
    Flammable - Keep away from fire or flame
    When using this product, avoid contact with eyes. In case of
    eye contact, rinse with water to remove.
    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

    . Wet hands thoroughly with product and allow to dry without wiping.

  • Inactive ingredients

    Aqua

  • PRINCIPAL DISPLAY PANEL

    NDC 76906-001-02 02

    NDC 76906-001-06 80

    NDC 76906-001-13 13

  • INGREDIENTS AND APPEARANCE
    WET WIPE 
    alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76906-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76906-001-0110 in 1 BAG02/04/2020
    15 g in 1 POUCH; Type 0: Not a Combination Product
    2NDC:76906-001-0220 in 1 BAG02/04/2020
    25 g in 1 POUCH; Type 0: Not a Combination Product
    3NDC:76906-001-0325 in 1 BAG02/04/2020
    35 g in 1 POUCH; Type 0: Not a Combination Product
    4NDC:76906-001-0450 in 1 BAG02/04/2020
    45 g in 1 POUCH; Type 0: Not a Combination Product
    5NDC:76906-001-05350 in 1 BAG02/04/2020
    55 g in 1 POUCH; Type 0: Not a Combination Product
    6NDC:76906-001-0680 in 1 BAG02/04/2020
    65 g in 1 POUCH; Type 0: Not a Combination Product
    7NDC:76906-001-07100 in 1 BAG02/04/2020
    75 g in 1 POUCH; Type 0: Not a Combination Product
    8NDC:76906-001-08135 in 1 BAG02/04/2020
    85 g in 1 POUCH; Type 0: Not a Combination Product
    9NDC:76906-001-09250 in 1 BAG02/04/2020
    95 g in 1 POUCH; Type 0: Not a Combination Product
    10NDC:76906-001-1310 in 1 BAG02/04/2020
    105 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A02/04/2020
    Labeler - Zhejiang BeiTao Hygienic Products Co., Ltd. (412925352)
    Registrant - Zhejiang BeiTao Hygienic Products Co., Ltd. (412925352)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang BeiTao Hygienic Products Co., Ltd.412925352manufacture(76906-001) , label(76906-001)
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