Label: 75% ALCOHOL DISINFECTANT liquid

  • 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 May 13, 2020

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

  • DOSAGE & ADMINISTRATION

    Keep it tightly closed and protected from light

  • INACTIVE INGREDIENT

    Purified water

  • INDICATIONS & USAGE

    1. Skin disinfection: Scrub disinfection of the original solution, the action time is 1-3 minutes
    2. Disinfection of the surface of the object: the original solution wipes and soaks the disinfected items, and the effect is 1.5-3

  • ACTIVE INGREDIENT

    ethanol

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of children

  • PURPOSE

    Disinfection
    Sterilization

  • WARNINGS

    1. This product is for external use and should not be taken orally;
    2. Use with caution to those who are allergic to ethanol;
    3. Keep it tightly closed and protected from light; .
    4. This product is flammable. It should be kept away from fire sources;
    5. The validity period is 24 months.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    75% ALCOHOL DISINFECTANT 
    75% alcohol disinfectant liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:40796-001
    Route of AdministrationEXTRACORPOREAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL375 mL  in 500 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code economical
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:40796-001-01500 mL in 1 BOTTLE; Type 0: Not a Combination Product05/13/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/13/2020
    Labeler - Jiangxi Baiyi Weishi Medical Technology Co., Ltd. (407967698)
    Establishment
    NameAddressID/FEIBusiness Operations
    Jiangxi Baiyi Weishi Medical Technology Co., Ltd.407967698manufacture(40796-001)