Label: ALCOHOL WIPE- alcohol cloth

  • 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 September 28, 2020

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

  • Drug Facts

  • Active Ingredient

    Ethyl Alcohol 75% (v/v)

    purpose

    Antiseptic

  • Uses

    • to decrease bacteria on the skin
  • Warnings

    • For External use only
    • Flammable,keep away from fire or flame
    • Flammable,keep away from fire or flame

    Do not use

    • with  electrocautcry procedures or in eyes

    Stop use if redness or irritation develops If

    condition continues for more than 72 hours consult a physician

    Keep out of reach of children

    in case of accidental ingestion,seek proffessional assistance or contact a Poision Control Center right away

  • Directions

    • Apply to clean and sterilizc hands, household and office objects,cellphone, computers,desks etc, and discard.
  • Inactive ingredient

    Purified Water 

  • Package Labeling:

    Bottle2

  • INGREDIENTS AND APPEARANCE
    ALCOHOL WIPE 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74979-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.75 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74979-004-011 in 1 PACKET08/20/2020
    12.4 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E08/20/2020
    Labeler - Robert Gordon Ind. Ltd. (070064709)