Label: MARVEL SPIDERMAN HAND SANITIZER WITH CASE- alcohol solution

  • NDC Code(s): 74530-044-01
  • Packager: Best Brand Consumers Products, Inc.
  • 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 January 2, 2022

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  • Active Ingredient(s)

    Ethyl Alcohol 68%

  • Purpose

    Antiseptic

  • Use

    To decrease the bacteria on the skin that could cause disease

    Recommended for repeated use

  • Warnings

    For external use only.

    Flammable. Keep away from heat and flame

    Discontinue if skin becomes irritated and ask a doctor

  • WHEN USING

    Keep out of eyes. In case of contact with eyes, flush thoroughly with water

    Do not inhale or ingest

    Avoid contact with broken skin

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of accidental ingestion, seek professional assitance or contact a Poison Control Center immediately.

  • Directions

    Wet hands thoroughly with products and rub untill dry withour wiping

    For children under 6, use only under adult supervision

    Not recommended for infants

  • Other information

    Do not store above 105F

    May discolor some fabrics

    Harmful to wooden finishes and plastics

  • Inactive ingredients

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

  • PRINCIPAL DISPLAY PANEL

    image description

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    MARVEL SPIDERMAN HAND SANITIZER WITH CASE 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74530-044
    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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    WATER (UNII: 059QF0KO0R)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74530-044-0129 mL in 1 BOTTLE; Type 0: Not a Combination Product09/25/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/25/2020
    Labeler - Best Brand Consumers Products, Inc. (058304494)
    Establishment
    NameAddressID/FEIBusiness Operations
    Huizhou Bliss Commodity Co., Ltd417467331manufacture(74530-044)
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