Label: BABY PANDA HAND SANITIZER- isopropyl alcohol spray

  • 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 July 6, 2020

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  • Drug Facts

  • Active Ingredient

    Isopropyl Alcohol 70%

  • Purpose

    Antimicrobial

  • USE

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

    • Do not use in the eyes. In case of contact rinse thoroughly with water
    • Do not use on children less than 2 months of age.
    • For external use only.
    • Flammable, keep away from heat and flame.
    • Stop use and ask doctor if 
    • Irritation and redness develop and persist for more than 72hrs
    • Swallowed, get medical attention or contact poison control center right away.

    Keep Out of Reach Of Children. Children must be supervised in use of this product.

  • Directions:

    • Spray product into palm to cover hands and rub hands together until dry.
    • Children under 6 years of age should be supervised when using this product.
  • Other Information:

    • Store below 110°F (43°C)
    • May discolor certain fabrics or surfaces
  • INACTIVE INGREDIENT

    Inactive Ingredients: Glycerin, Water, Coco-Caprylate, Citrs Aurantium Dulcis Peel Oil.

  • SPL UNCLASSIFIED SECTION

    Kills 99.9% of Germs and Bacteria

    See info for purity*

    A portion of the proceeds donated to WWF.    

    NO ANIMAL TESTING

    Made in the USA 

    Distributed By:

    Dermapeutics Corp

    Calabasas, CA 91302

    WWW.DERMAPEUTICS.COM

  • Packaging

    IMAGE

  • INGREDIENTS AND APPEARANCE
    BABY PANDA HAND SANITIZER 
    isopropyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79416-557
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H)  
    ORANGE OIL (UNII: AKN3KSD11B)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79416-557-01120 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/07/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/07/2020
    Labeler - Dermapeutics (859082237)
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