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Ethyl Rubbing Alcohol by Humco Holding Group, Inc.

Medically reviewed on December 30, 2017

Dosage form: liquid
Ingredients: ALCOHOL 700mg in 1mL
Labeler: Humco Holding Group, Inc.
NDC Code: 0395-0040

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.

Ethyl Rubbing Alcohol

HUMCO Ethyl Rubbing Alcohol 70%, USP

Drug Facts

Active Ingredient

Ethyl 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 away 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 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
  • will produce serious gastric disturbances if taken internally.

Inactive Ingredient

Acetone 5%

Methyl isobutyl ketone 1%

bitrex

purified water

Principal Display Panel

NDC 0395-0040-16
RUBBING ALCOHOL
ETHYL ALCOHOL
70%
USP

First Aid Antiseptic
16 fl oz (1 pt) 473 mL

New Label

ETHYL RUBBING ALCOHOL 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0395-0040
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL700 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ACETONE50 mg  in 1 mL
METHYL ISOBUTYL KETONE10 mg  in 1 mL
DENATONIUM BENZOATE 
WATER 
Packaging
#Item CodePackage Description
1NDC:0395-0040-16473 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/1997
Labeler - Humco Holding Group, Inc. (825672884)
Registrant - Humco Holding Group, Inc. (825672884)
Establishment
NameAddressID/FEIOperations
Humco Holding Group, Inc.825672884manufacture(0395-0040), analysis(0395-0040), pack(0395-0040), label(0395-0040)

 
Humco Holding Group, 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.

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