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Sunmark Isopropyl Rubbing Alcohol 70 Percent

Medically reviewed on December 13, 2017

Dosage form: liquid
Ingredients: ISOPROPYL ALCOHOL 700mg in 1mL
Labeler: McKesson
NDC Code: 49348-173

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 Rubbing Alcohol 70 Percent USP

Drug Facts

Active Ingredient

Isopropyl Alcohol 70% by volume

Purpose

First aid antiseptic

Use

First aid to help prevent the risk of infection in.

  • minor cuts
  • scrapes
  • burns

Warnings

For external use only.

  • Flammable, keep way from spark, heat and flame.
  • Use in well ventilated area, fumes may be harmful.

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

When using this product
  • do not get into eyes or mucous membranes.
  • do not apply to irritated skin.

Stop use and ask a doctor if

excessive irritation of the skin develops.

Keep out of reach of children.

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

Directions
  • 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 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 49348-173-38
isopropyl rubbing

alcohol

70% USP

16 FL OZ (1 PT) 473 mL

SUNMARK ISOPROPYL RUBBING ALCOHOL 70 PERCENT 
isopropyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49348-173
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL) ISOPROPYL ALCOHOL700 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
Packaging
#Item CodePackage Description
1NDC:49348-173-38473 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)
Establishment
NameAddressID/FEIOperations
Humco Holding Group, Inc.825672884analysis(49348-173), manufacture(49348-173), pack(49348-173), label(49348-173)

 
McKesson

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.

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