Label: ISOPROPYL ALCOHOL 91%- isopropyl 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 July 21, 2022

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

View All Sections
  • Drug Facts

  • Active Ingredients (by volume)

    Isopropyl Alcohol, 91%

    Purpose

    First Aid Antiseptic

  • Use[s]

    first aid to help prevent the risk of infection in minor cuts, scrapes, and burns.

  • Warnings

    For external use only. Flammable.

    • Keep away from fire, flame, heat, spark, electricity.
    • If taken internally, serious gastric disturbances will result.
    • Use only in well ventilated area; fumes may be toxic.

    Ask a doctor before use if you have

    deep or puncture 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 week unless directed by a doctor.

    Stop use and ask a doctor if

    • condition persists or gets worse
    • do not use other-wise than directed

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

  • Directions

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

    • Store at room temperature does not contain, nor is intended as a substitute for grain or ethyl alcohol
  • Inactive ingredients

    Purified water

  • Questions or comments?

    Call 1-855-238-4488

  • Packag Labeling:

    Bottle

  • INGREDIENTS AND APPEARANCE
    ISOPROPYL ALCOHOL 91% 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78706-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.91 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78706-002-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product09/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E09/01/2020
    Labeler - Virgin Scent Inc. (034474058)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!