Label: ISOPROPYL ALCOHOL liquid

  • Category: HUMAN OTC DRUG LABEL

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 January 17, 2022

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • PURPOSE

    Antiseptic

  • INDICATIONS & USAGE

    Directions: Apply to affected area for first-aid treatment of minor cuts and abrasions.  In case of deep or puncture wounds consult a physician.  Discontinue use and get medical aid if redness, irritation or infection develops.  Apply liberally for rubbing.

  • ACTIVE INGREDIENT

    Active ingredient:  Isopropyl alcohol, 70%

  • KEEP OUT OF REACH OF CHILDREN

    Warnings:  For external use only.  Avoid contact with eyes or mucous membranes.  Ingestion will result in gastrointestinal distress, unconsciousness and death.  Keep out of reach of children.  In case of ingestion contact a poison control center immediately.

  • USER SAFETY WARNINGS

    Flammable: Avoid sources of ignition.  Do not use around open flames.

  • WARNINGS

    Warnings:  For external use only.  Avoid contact with eyes or mucous membranes.  Ingestion will result in gastrointestinal distress, unconsciousness and death.  Keep out of reach of children.  In case of ingestion contact a poison control center immediately.

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water

  • DOSAGE & ADMINISTRATION

    Directions:  Apply to affected area for first-aid treatment of minor cuts and abrasions.  In case of deep or puncture wounds consult a physician.  Discontinue use and get medical aid if redness, irritation or infection develops.  Apply liberally for rubbing.

  • PRINCIPAL DISPLAY PANEL

    ipa70label.jpg
    ipa70label




  • INGREDIENTS AND APPEARANCE
    ISOPROPYL ALCOHOL 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12745-105
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70.14 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:12745-105-01946 mL in 1 BOTTLE, PLASTIC; Type 1: Convenience Kit of Co-Package06/15/1954
    2NDC:12745-105-033785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/15/1954
    3NDC:12745-105-043785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/15/1954
    4NDC:12745-105-0518927 mL in 1 CONTAINER; Type 0: Not a Combination Product06/15/1954
    5NDC:12745-105-0618927 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product06/15/1954
    6NDC:12745-105-07208198 mL in 1 DRUM; Type 0: Not a Combination Product06/15/1954
    7NDC:12745-105-08473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/15/1954
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34406/15/1954
    Labeler - Medical Chemical Corporation (008496861)
    Establishment
    NameAddressID/FEIBusiness Operations
    Medical Chemical Corporation008496861manufacture(12745-105)
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

More Info on this Drug

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