Label: ISOPROPYL RUBBING ALCOHOL- isopropyl alcohol solution

  • NDC Code(s): 43128-002-01, 43128-002-16, 43128-002-32
  • Packager: NDC, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 15, 2024

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

View All Sections
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Isopropyl Alcohol 70% v/v

  • Purpose

    First Aid Antiseptic

  • Uses

    First aid to help prevent the risk of infection in:

    • minor cuts
    • scrapes
    • burns
  • WARNINGS

    For external use only

    Flammable

    • keep away from fire or flame, heat, spark, electrical. Flash point 72°F
    • do not use with electrocautery procedures.

    Ask a doctor before use if you havedeep 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 1 week unless directed by a doctor

    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 infected area
    • apply 1 to 3 times daily
  • Other information

    • does not contain, nor is intended as a substitute for grain or ethyl alcohol
    • will produce serious gastric disturbances if taken internally
  • Inactive Ingredient

    Purified Water

  • PRINCIPAL DISPLAY PANEL 

    REF: P907132

    NDC 43128-002-32

    Pro
    ADVANTAGE®

    Isopropyl Rubbing
    Alcohol 70% USP

    Tamper evident cap for your protection.
    If ring-band is detached from cap or missing do not use.

    WARNING:Flammable

    Made in USA for:
    NDC, Inc., 407 New Sanford Rd.
    La Vergne, TN 37086
    www.ProAdvantagebyNDC.com

    32 fl. oz. (946 mL)

    PRINCIPAL DISPLAY PANEL

  • INGREDIENTS AND APPEARANCE
    ISOPROPYL RUBBING ALCOHOL 
    isopropyl alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43128-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43128-002-32946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2014
    2NDC:43128-002-013785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2014
    3NDC:43128-002-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00306/01/2014
    Labeler - NDC, Inc. (009831413)
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!