Label: D.THERAPINO KAMOO HAND SANITIZER- 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 11, 2020

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  • ACTIVE INGREDIENT

    alcohol

  • INACTIVE INGREDIENT

    water, aloe extract, carbomer, menthol, triethanolamine

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF THE CHILDREN

  • PURPOSE

    hand sanitizer to help reduce bacteria that potentially can cause disease

    for use when soap and water are not available

  • INDICATIONS & USAGE

    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.

  • WARNINGS

    For external use only.

    Flammable, keep away from fire or flame.

    When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.

    Stop use and ask a doctor if significant irritation or sensitization develops.

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

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    D.THERAPINO KAMOO HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58241-0002
    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
    MENTHOL (UNII: L7T10EIP3A)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58241-0002-150 mL in 1 BOTTLE; Type 0: Not a Combination Product04/11/2020
    2NDC:58241-0002-280 mL in 1 BOTTLE; Type 0: Not a Combination Product04/11/2020
    3NDC:58241-0002-3500 mL in 1 BOTTLE; Type 0: Not a Combination Product04/11/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/11/2020
    Labeler - David Cosmetic Co Ltd (695697845)
    Registrant - David Cosmetic Co Ltd (695697845)
    Establishment
    NameAddressID/FEIBusiness Operations
    David Cosmetic Co Ltd695697845manufacture(58241-0002) , label(58241-0002)
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