Label: 75% ALCOHOL DISINFECTANT- alcohol liquid

  • NDC Code(s): 41366-015-01
  • Packager: Zhejiang Meimi Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 20, 2024

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  • Active Ingredient(s)

    Ethyl Alcohol 75% v/v

  • Purpose

    Antiseptic

  • Use

    Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

  • Warnings

    • For external use only.
    • Flammable. Keep away from heat or flame.
  • Do not use

    • in children less than 2 months of age
    • on open skin wounds
  • WHEN USING

    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

  • STOP USE

    Stop use and ask a doctor if irritation or rash occurs.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Place enough product on hands to cover all surfaces. Rub hands together until dry.
    • Supervise children under 6 years of age when using this product to avoid swallowing.
  • Other information

    • Store between 15-30℃(59-86℉)
    • Avoid freezing and excessive heat above 40℃(104℉)

  • Inactive ingredients

    Water(Aqua, Eau).

  • Package Label - Principal Display Panel

    88 mL in 1 BOTTLE NDC: 41366-015-01 88ml label

  • INGREDIENTS AND APPEARANCE
    75% ALCOHOL DISINFECTANT 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41366-015
    Route of AdministrationEXTRACORPOREAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41366-015-0188 mL in 1 BOTTLE; Type 0: Not a Combination Product08/16/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/16/2020
    Labeler - Zhejiang Meimi Technology Co., Ltd. (413668440)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Meimi Technology Co., Ltd.413668440manufacture(41366-015)
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