Label: ALCOHOL GLOBAL CARE (ETHYL)- alcohol 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 August 10, 2020

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  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 70%

    Purpose

    First aid antiseptic

  • USE

    helps prevent the risk of infections in minor cuts, scrapes and burns

  • Warning

    For external use only.

    Flammable. Keep away from fire or flame, heat, spark, electrical

    USE ONLY IN A WELL-VENTILATED AREA;FUMES MAY BE HARMFUL

    Ask doctor before use

    for deep wounds, animal bites or serious burns

    When using this product

    • do not get into eyes
    • do not apply over large areas of the body
    • do not use longer than 1 week

    Stop use and ask a doctor if

    the condition persists or gets worse

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • clean affected areas
    • apply 1 to 3 times daily
  • Inactive ingredients

    Softened Water

  • Other information:

    store at controlled room temperature

    • will produce serious gastric disturbances if taken internally
  • Package Labeling:946ml

    Bottle3

  • Package Labeling:3785.41ml

    Bottle4

  • INGREDIENTS AND APPEARANCE
    ALCOHOL GLOBAL CARE (ETHYL) 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72146-032
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72146-032-01946 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2020
    2NDC:72146-032-023785.41 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E08/01/2020
    Labeler - TARGET PRICE INC (081086884)
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