Label: 75% ALCOHOL DISNFECTANT 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 March 2, 2022

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  • Active ingredient

    Ethyl alcohol 75% v/v. Purpose: Antiseptic

  • Purpose

    Antiseptic

  • Uses

    to decrease bacteria on the skin that could cause disease

    recommended for repeated use.

  • Warnings

    For external use only

    Flammable

    Keep away from fire or flame

  • DO NOT USE

  • WHEN USING

    keep out of eyes.In case of contact with eyes,flush thoroughly with water.

    avoid contact with broken skin

    do not inhale or ingest

  • STOP USE

    irritation or redness develops

    condition persists for more than 72 hours.

  • KEEP OUT OF REACH OF CHILDREN

    If swallowed, get medical heip 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

    Do not store above 105ºF

    May discolor some fabrics

    Harmful to wood finishes and piastics.

  • Inactive ingredients

    Water.

  • PRINCIPAL DISPLAY PANEL

    60mL NDC:73905-011-01 60mL

    300mL NDC:73905-011-02 300mL

  • INGREDIENTS AND APPEARANCE
    75% ALCOHOL DISNFECTANT 
    75% alcohol disnfectant liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73905-011
    Route of AdministrationTOPICAL
    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:73905-011-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    2NDC:73905-011-02300 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/30/2020
    Labeler - ZHEJIANG JINGHUI COSMETICS SHARE CO.,LTD (529558167)
    Establishment
    NameAddressID/FEIBusiness Operations
    ZHEJIANG JINGHUI COSMETICS SHARE CO.,LTD529558167manufacture(73905-011)
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