ETHYL RUBBING ALCOHOL- alcohol liquid

Ethyl Rubbing Alcohol by

Drug Labeling and Warnings

Ethyl Rubbing Alcohol by is a Otc medication manufactured, distributed, or labeled by Humco Holding Group, Inc., Pharma Nobis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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

INGREDIENTS AND APPEARANCE

ETHYL RUBBING ALCOHOL 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0395-0040
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	700 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ACETONE (UNII: 1364PS73AF)	50 mg  in 1 mL
METHYL ISOBUTYL KETONE (UNII: U5T7B88CNP)	10 mg  in 1 mL
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0395-0040-16	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/1997

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/1997

Labeler - Humco Holding Group, Inc. (825672884)

Registrant - Humco Holding Group, Inc. (825672884)

Establishment
Name	Address	ID/FEI	Business Operations
Humco Holding Group, Inc.		825672884	manufacture(0395-0040) , analysis(0395-0040) , pack(0395-0040) , label(0395-0040)