Label: ANTIBACTERIAL HAND SANITIZER 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 August 19, 2020

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

  • Active Ingredient

    Active lngredient:Isopropyl Alcohol

  • Purpose

    /

  • Uses

    No water needed.

  • Warnings

    /

  • DO NOT USE

    /

  • WHEN USING THIS PRODUCT

    /

  • STOP USE

    /

  • KEEP OUT OF REACH OF CHILDREN

    /

  • Directions

    No water needed.Apply a small amount of product to dry skin. Rub briskiy. Wipe with paper towel or clean cloth or rinse with water and dry .

  • Other information

    /

  • Inactive ingredients

    Alcohol ,Aloe Vera GeL,
    Extracts of Juniper ,Eucalyptus OiL,
    Thymol,Essence (Radix), Carbomer,
    Diisopropanol Amine ,Purified Water.

  • Package Label - Principal Display Panel

    74881-007-01 3.7ml

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL HAND SANITIZER 
    antibacterial hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74881-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    DIISOPROPANOLAMINE (UNII: 0W44HYL8T5)  
    JUNIPER BERRY (UNII: O84B5194RL)  
    THYMOL (UNII: 3J50XA376E)  
    METHYL BENZOATE (UNII: 6618K1VJ9T)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74881-007-013.7 mL in 1 POUCH; Type 0: Not a Combination Product07/27/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/27/2020
    Labeler - Huizhou Baozi Biotechnology Co., Ltd. (419304583)
    Registrant - Huizhou Baozi Biotechnology Co., Ltd. (419304583)
    Establishment
    NameAddressID/FEIBusiness Operations
    Huizhou Baozi Biotechnology Co., Ltd.419304583manufacture(74881-007)