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Isopropyl Alcohol by Medline Industries, Inc.

Dosage form: liquid
Ingredients: ISOPROPYL ALCOHOL 70mL in 100mL
Labeler: Medline Industries, Inc.
NDC Code: 53329-800

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 Facts

Active ingredient

Isopropyl Alcohol 70%


First Aid Antiseptic


For first aid to help prevent the risk of infection in minor:

  • cuts
  • scrapes
  • burns


For external use only.

Flammable. Keep away from fire or flame.

Do not use

with electrocautery procedures. Use only in a well ventilated area; fumes may be toxic

When using this product do not
  • get into eyes
  • apply over large areas of the body. In case of deep or puncture wounds, animal bites or serious burns, consult a doctor.

Stop use and ask a doctor if

condition persists or gets worse or lasts for more than 72 hours. Do not use longer than 1 week unless directed by a doctor.

Keep out of reach of children.

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

  • Clean the affected area. Apply a small amount of the product on the area 1 to 3 times daily.
  • May be covered with a sterile bandage.
  • If bandaged, let dry first.

Other Information
  • Does not contain, nor is intended as a substitute for grain or ethyl alcohol.
  • Will produce serious gastric disturbances if taken internally.
  • Protect from freezing and avoid excessive heat.

Inactive ingredients


Package/Label Principal Display Panel


NDC: 53329-800-06


Isopropyl Alcohol

First Aid Antiseptic



Keep away from heat, spark, electrical fire of flame

Use only in a well-ventilated area; fumes can be harmful

16 FL OZ

(1 PT) 473 mL

isopropyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-800
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:53329-800-06473 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A02/16/2009
Labeler - Medline Industries, Inc. (025460908)

Revised: 05/2016
Medline Industries, Inc.

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.