Label: HAND SANITIZER ANTIBACTERIAL GEL gel

  • 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 7, 2020

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

  • Active Ingredien


    Ethyl Alcohol 70% Antiseptic

  • Keep out of reach of children

    If swallowed, contact a physician or poison control center.

  • purpose


    Antiseptic

  • Warnings


    External use only, Not to take orally.

    seek professional help if skin gets allergic to the alcohol

  • Inactive ingredients

  • DISPOSAL AND WASTE HANDLING

    Do not sote above 110 oF

  • INDICATIONS&USAGE

    Apply a few drops of gel on the hand and rub them thoroughly.

  • DOSAGE&ADMINISTRATION

    29ML

  • PACKAGE LABEL

    label

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER ANTIBACTERIAL GEL 
    hand sanitizer antibacterial gel gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72922-012
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALOE (UNII: V5VD430YW9)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72922-012-0159 mL in 1 BOTTLE; Type 0: Not a Combination Product03/04/2019
    2NDC:72922-012-0252 mL in 1 BOTTLE; Type 0: Not a Combination Product03/04/2019
    3NDC:72922-012-03240 mL in 1 BOTTLE; Type 0: Not a Combination Product03/04/2019
    4NDC:72922-012-04100 mL in 1 BOTTLE; Type 0: Not a Combination Product03/04/2019
    5NDC:72922-012-05500 mL in 1 BOTTLE; Type 0: Not a Combination Product03/04/2019
    6NDC:72922-012-063785 mL in 1 BOTTLE; Type 0: Not a Combination Product03/04/2019
    7NDC:72922-012-0729 mL in 1 BOTTLE; Type 0: Not a Combination Product03/04/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/04/2019
    Labeler - ShangRao chunyu Technology CO.,LTD. (541569308)
    Establishment
    NameAddressID/FEIBusiness Operations
    ShangRao chunyu Technology CO.,LTD.541569308manufacture(72922-012)