Label: MICKEY MOUSE HAND SANITIZER- alcohol solution

  • NDC Code(s): 74274-003-01, 74274-003-02
  • Packager: Huizhou Bliss Commodity Co., Ltd
  • 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 June 9, 2020

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  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 68%

  • Purpose

     Antiseptic

  • Use

    • Decreases bacteria on the skin that could cause disease.
    • Recommended for repeated use.
  • Warnings

    • For external use only.
    • Flammable.Keep product away from heat or flame.
    • Discontinue if skin becomes irritated and ask a doctor
    • Keep out of reach of children.
    • In case of accidental ingestion seek professional assistance or contact a Poison Control Center immediately.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Wet hands thoroughly with product and rub until dry without wiping.
    • For children under 6, use only under adult supervison.
    • Not recommended for infants.
  • Inactive ingredients

    Water, glycerin, propyene glycol, carbomer, sodium hydroxide, fragrance

  • SPL UNCLASSIFIED SECTION

    other information:

    • Do not store above 105 Fahrenheit degree
    • May discolor some fabrics
    • Harmful to wood finishes and plastics
  • Packaging

    image description

  • INGREDIENTS AND APPEARANCE
    MICKEY MOUSE HAND SANITIZER 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74274-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL68 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74274-003-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product03/31/2020
    2NDC:74274-003-0230 mL in 1 BOTTLE; Type 0: Not a Combination Product06/09/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E03/31/2020
    Labeler - Huizhou Bliss Commodity Co., Ltd (417467331)
    Registrant - Huizhou Bliss Commodity Co., Ltd (417467331)
    Establishment
    NameAddressID/FEIBusiness Operations
    Huizhou Bliss Commodity Co., Ltd417467331manufacture(74274-003)
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