Label: BEAUTAIME HAND DOCTOR- alcohol gel

  • 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 April 18, 2020

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  • ACTIVE INGREDIENT

    Active ingredients: ETHANOL 62.0% w/w

  • INACTIVE INGREDIENT

    Inactive ingredients

    Water, Glycerin, Propylene Glycol, Triethanolamine, Carbomer, Aloe Barbadensis Leaf Powder, Aloe Extract

  • PURPOSE

    Purpose: ANTISEPTIC

  • WARNINGS

    Warnings

    For external use only. Flammable. Keep away from heat or flame
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    Do not use
    • in children less than 2 months of age
    • on open skin wounds
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    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
    --------------------------------------------------------------------------------------------------------
    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

  • KEEP OUT OF REACH OF CHILDREN

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

  • Uses

    Uses
    Hand sanitizer to help reduce bacteria that potentially can cause disease.

  • Directions

    Directions

    • Place enough product on hands to cover all surfaces. Rub hands together until dry.
    • Supervise children under 6 years of age when using this product to avoid swallowing.

  • Other information

    Other information
    • Store between 15-30C (59-86F)
    • Avoid freezing and excessive heat above 40C (104F)

  • PACKAGE LABEL - BEAUTAIME HAND DOCTOR GEL 70mL

    Image of container

  • PACKAGE LABEL - BEAUTAIME HAND DOCTOR GEL 500mL

    Image of bottle

  • INGREDIENTS AND APPEARANCE
    BEAUTAIME HAND DOCTOR 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73697-110
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Glycerin (UNII: PDC6A3C0OX)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Trolamine (UNII: 9O3K93S3TK)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ALOE (UNII: V5VD430YW9)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73697-110-0170 mL in 1 CONTAINER; Type 0: Not a Combination Product04/01/2020
    2NDC:73697-110-02500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/01/2020
    Labeler - ASAN C&S (631139649)
    Registrant - ASAN C&S (631139649)
    Establishment
    NameAddressID/FEIBusiness Operations
    ASAN C&S631139649manufacture(73697-110)