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Sunmark Isopropyl Alcohol 91 Percent

Medically reviewed on December 12, 2017

Dosage form: liquid
Ingredients: ISOPROPYL ALCOHOL 910mg in 1mL
Labeler: McKesson
NDC Code: 49348-174

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.

Sunmark Isopropyl Alcohol 91 Percent USP

Drug Facts

Active Ingredient

Isopropyl Alcohol 91% by volume


First aid antiseptic


First aid to help prevent the risk of infection in.

  • minor cuts
  • scrapes
  • burns


For external use only.

  • Flammable, keep way from spark, heat and flame.

Ask a doctor before use for
  • deep wounds
  • animal bites
  • 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

Stop use and ask a doctor if

If condition persists or gets worse.

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

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

Other Information
  • store at controlled room temperature
  • 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

NDC 49348-174-38
isopropyl rubbing


91% USP

16 FL OZ (1 PT) 473 mL

isopropyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49348-174
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:49348-174-38473 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/2016
Labeler - McKesson (177667227)
Registrant - Humco Holding Group, Inc. (825672884)
Humco Holding Group, Inc.825672884analysis(49348-174), manufacture(49348-174), pack(49348-174), label(49348-174)


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.