Label: 90013 HAND SANITIZER- alcohol solution

  • NDC Code(s): 74274-009-01
  • 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 April 18, 2020

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  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 68%

  • Purpose

     Antiseptic

  • Use

    For Hand Sanitizing

  • KEEP OUT OF REACH OF CHILDREN

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

  • warnings:

    Flamable, keep away from heat and flame.

    For external use only-hands.

    When using this product

    Keep out of eyes. In case of contact with eyes, Flush thoroughly with water. Avoid contact wieh broken skin. Do not inhale or ingest.

    Stop use and ask a doctor if skin irritation develops.

    Other Information

    • Do not store above 105℉
    • May discolor some fabrics.
  • Directions

    • Wet hands thoroughly with product and allow to dry without wiping.
    • For children under 6 age only under adult supervision.
    • Not recommended for infants.
  • Inactive ingredients

    Aqua, glycerin, carbomer, propyene glycol, sodium hydroxide

  • Packaging

    image description

  • INGREDIENTS AND APPEARANCE
    90013 HAND SANITIZER 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74274-009
    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:74274-009-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product04/18/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/18/2020
    Labeler - Huizhou Bliss Commodity Co., Ltd (417467331)
    Registrant - Huizhou Bliss Commodity Co., Ltd (417467331)
    Establishment
    NameAddressID/FEIBusiness Operations
    Huizhou Bliss Commodity Co., Ltd417467331manufacture(74274-009)
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