Label: DISNEY BAMBI MOISTURIZING HAND SANITIZER MELON- alcohol 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 December 9, 2021

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  • DRUG FACTS

  • Active Ingredient

    Ethylalcohol 69%

    Purpose

    Antimicrobial

  • Uses

    Reduce bacteria on hands.

  • Warnings

    Flammable. Keep away from source of Ignition or flame.

    For external use only.

    Do not use

    on open skin wounds

    When using this product

    keep out of eyes.

    Stop use and ask a doctor

    if irritation or redness develops.

    Keep out of reach of children.

    If swallowed, get medical help or contact a doctor immediately.

  • Directions

    Spray into hands. Rub until absorbed.

    Supervise children under 6 years of age when using this produt to avoid swallowing.

  • Inactive Ingredients

    Water(Aqua)/Eau, pentylene Glycol, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Butylene Glycol, Fragrance(parfum), Sodium Hydroxide, Aloe Barbadensis (Aloe Vera)Leaf Extract.

  • Other Information

    Store between 15-30°C (59-86°F). Avoid freezing and excessive heat above 40°C (104°F).

  • Questions or Comments

    MAD BEAUTY USA LLC

    1030 SALEM ROAD

    UNION NJ 07083 MARYLAND

    TEL (844) 995 1701

  • Package Labeling:

    Bottle12

  • INGREDIENTS AND APPEARANCE
    DISNEY BAMBI MOISTURIZING HAND SANITIZER MELON 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78789-022
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.69 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78789-022-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product07/20/202012/31/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E07/20/202012/31/2024
    Labeler - Mad Beauty USA LLC (117508758)
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