Label: ALLPEAU PURE HAND SANITIZER- alcohol hand sanitizer gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 April 27, 2020

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  • Active Ingredient(s)

    Alcohol 75% v/v. Purpose: Hand Sanitizer

  • Purpose

    Hand Sanitizer

  • Use

    Hand sanitizer to decrease on hands.

  • Warnings

    • For external use only.
    • Flammable. Keep away from heat and flame.

  • Do not use

    Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

  • WHEN USING

    When using this product do not use in or near the eyes.

    In case of contact, rinse eyes thoroughly with water.

  • STOP USE

    Stop use and ask a doctor if irritation and redness develops and lasts.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help immediately.

  • Directions

    • Take proper amount of product into the palm and rub hands together until dry.
    • Supervise children under 6 years in the use of the product. Not recommended for infants.
  • Other information

    Store below 110℉ (43℃).

    May discolor certain fabrics or surfaces.

  • Inactive ingredients

    water, acrylates/vinyl isodecanoate crosspolymer, propylene glycol, triethanolamine, aloe barbadensis extract, cucumis sativus extract, houttuynia cordata extract, parfum, CI 42090, CI 19140

  • Package Label - Principal Display Panel

    60

  • INGREDIENTS AND APPEARANCE
    ALLPEAU PURE HAND SANITIZER 
    alcohol hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75567-1011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL42 mL  in 60 mL
    Inactive Ingredients
    Ingredient NameStrength
    HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    CUCUMBER (UNII: YY7C30VXJT)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75567-1011-160 mL in 1 BOTTLE; Type 0: Not a Combination Product04/27/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/27/2020
    Labeler - WID Cosmetics (Shanghai) Co., Ltd. (554443373)
    Registrant - A03 Lab of BTS (548009541)
    Establishment
    NameAddressID/FEIBusiness Operations
    WID Cosmetics (Shanghai) Co., Ltd.554443373manufacture(75567-1011) , label(75567-1011)
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