ISOPROPYL ALCOHOL 91%- isopropyl alcohol liquid

Isopropyl Alcohol 91% by

Drug Labeling and Warnings

Isopropyl Alcohol 91% by is a Otc medication manufactured, distributed, or labeled by Virgin Scent Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients (by volume)

Isopropyl Alcohol, 91%

Purpose

First Aid Antiseptic

Use[s]

first aid to help prevent the risk of infection in minor cuts, scrapes, and burns.

Warnings

For external use only. Flammable.

• Keep away from fire, flame, heat, spark, electricity.
• If taken internally, serious gastric disturbances will result.
• Use only in well ventilated area; fumes may be toxic.

Ask a doctor before use if you have

deep or puncture wounds, animal bites or 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 week unless directed by a doctor.

Stop use and ask a doctor if

• condition persists or gets worse
• do not use other-wise than directed

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Directions

• clean the affected area
• apply a small amount of this product on the area 1 to 3 times daily
• if bandaged, let dry first 
• may be covered with a sterile bandage

Other information

• Store at room temperature does not contain, nor is intended as a substitute for grain or ethyl alcohol

Inactive ingredients

Purified water

Questions or comments?

Call 1-855-238-4488

Packag Labeling:

INGREDIENTS AND APPEARANCE

ISOPROPYL ALCOHOL 91% 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78706-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.91 mL  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78706-002-16	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	09/01/2020

Labeler - Virgin Scent Inc. (034474058)