Label: CVS HEALTH ISOPROPYL RUBBING ALCOHOL- isopropyl alcohol aerosol, spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 22, 2024

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  • Drug Facts

  • Active ingredient

    Isopropyl alcohol 70% by volume

    Purpose

    First aid antiseptic

  • Uses

    • first aid to help prevent the risk of infection in minor cuts, scrapes and burns
    • helps relieve minor muscular aches due to exertion
  • Warnings

    For external use only. Flammable,keep away from heat, spark, electrical, fire or flame 

    • will produce serious gastric disturbances if taken internally

    Do not use

    • in the eyes or apply over large areas of the body 
    • longer than 1 week 
    • do not inhale

    Ask a doctor before use if you have

    deep or puncture wounds, animal bites or serious burns.

    Stop use and ask a doctor if

    • the condition persists or gets worse 
    • irritation, pain, or redness persists or worsens 
    • swelling, rash, or fever develops

    Keep out of reach of children.

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

  • Directions

    • clean the affected area 
    • apply a small amount of product on the affected area 1 to 3 times a day 
    • may be covered with a sterile bandage 
    • if bandaged, let dry first
  • Other information

    • keep tightly closed and at controlled room temperature 
    • does not contain, nor is it intended as a substitute for grain or ethyl alcohol
  • Inactive ingredients

    Nitrogen, Purified Water, Sodium Benzoate

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    CVS HEALTH ISOPROPYL RUBBING ALCOHOL 
    isopropyl alcohol aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51316-979
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    NITROGEN (UNII: N762921K75)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51316-979-0085 g in 1 CONTAINER; Type 0: Not a Combination Product03/19/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/19/2024
    Labeler - CVS Pharmacy, Inc (062312574)
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