IDO DISINFECTION ETHANOL- isopropyl alcohol liquid

IDO DISINFECTION ETHANOL by

Drug Labeling and Warnings

IDO DISINFECTION ETHANOL by is a Otc medication manufactured, distributed, or labeled by IDO PHARM. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Isopropyl Alcohol

INACTIVE INGREDIENT

Water

PURPOSE

First aid to help prevent the risk of infection in minor cuts, scrapes or burns.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

INDICATIONS & USAGE

For the external use only

WARNINGS

For external use only

• If taken internally, serious gastric disturbances will result
• flammable, keep away from heat or flame

Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns

When using this product

• do not use in or near eyes. In case of contact with eyes, rinse eyes thoroughly with water
• do not apply over large areas of the body
• do not use longer than one week unless directed by a doctor

Stop use and ask a doctor if irritation or rash appears

Keep out of reach of children. In case of ingestion, get medical help or contact a Poison Control Center 1-800-222-1222 or dial 911 immediately

DOSAGE & ADMINISTRATION

Clean affected area

Apply small amount of this product on the affected area 1-3 times daily

May be covered with a sterile bandage. If bandaged, let dry first

children under 6 years of age should be supervised when using this product

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

IDO DISINFECTION ETHANOL 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77039-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	83 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77039-020-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/01/2022

Labeler - IDO PHARM (694853523)

Registrant - IDO PHARM (694853523)

Establishment
Name	Address	ID/FEI	Business Operations
IDO PHARM		694853523	manufacture(77039-020)