Label: INSTANT HAND SANITIZER- alcohol solution

  • NDC Code(s): 74274-005-01
  • Packager: Huizhou Bliss Commodity Co., Ltd
  • 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 April 24, 2020

If you are a consumer or patient please visit this version.

  • Drug Facts

  • Active ingredient

    Ethyl Alcohol   65%

  • 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 flames

    For external use only

    When using this product

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

    Stop and ask a doctor

    if skin irritation develops.

  • Directions

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

    Other information

    • Do not store above 105℉。
    • May discolor some fabrics.
  • Inactive ingredients

    Aqua, glycerin, carbomer, propyene glycol, sodium hydroxide.

  • Packaging

    image description

  • INGREDIENTS AND APPEARANCE
    INSTANT HAND SANITIZER 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74274-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65 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:74274-005-01500 mL in 1 BOTTLE; Type 0: Not a Combination Product04/24/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/24/2020
    Labeler - Huizhou Bliss Commodity Co., Ltd (417467331)
    Registrant - Huizhou Bliss Commodity Co., Ltd (417467331)
    Establishment
    NameAddressID/FEIBusiness Operations
    Huizhou Bliss Commodity Co., Ltd417467331manufacture(74274-005)