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HUMCO Isopropyl Rubbing Alcohol 70%

Medically reviewed on November 14, 2017.

Dosage form: liquid
Ingredients: ISOPROPYL ALCOHOL 700mg in 1mL
Labeler: Humco Holding Group, Inc.
NDC Code: 0395-1249

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.

HUMCO Isopropyl Rubbing Alcohol 70%, 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.

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

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.

Directions
  • clean the affected area.
  • apply a smal 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 distrurbances if taken internally.

Inactive Ingredient

purified water

Principal Display Panel

Label 16 fl oz

Principal Display Panel

Label 1 Gal

HUMCO ISOPROPYL RUBBING ALCOHOL 70% 
isopropyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0395-1249
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:0395-1249-16473 mL in 1 BOTTLE, PLASTIC
2NDC:0395-1249-283800 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/2008
Labeler - Humco Holding Group, Inc. (825672884)
Registrant - Humco Holding Group, Inc. (825672884)
Establishment
NameAddressID/FEIOperations
Humco Holding Group, Inc.825672884manufacture(0395-1249), analysis(0395-1249), pack(0395-1249), label(0395-1249)

 
Humco Holding Group, Inc.

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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