ISOPROPYL ALCOHOL liquid

ISOPROPYL ALCOHOL by

Drug Labeling and Warnings

ISOPROPYL ALCOHOL by is a Otc medication manufactured, distributed, or labeled by Degasa, S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Isopropyl alcohol 91%

Purpose

First Aid Antiseptic

Inactive Ingredients

Water

Uses

First aid to help prevent the risk of infection in:

• Minor cuts
• Scrapes
• Burns

Warnings

For external use onlyFlammable

• Keep away from fire or flame, heat, spark, electrical

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 inhale
• 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.

If swallowed, get medical help or contact a Poison Control Center right away.

Caution

Fumes can be acutely irritating to skin, eyes and the respiratory system. Do not apply to irritated skin or if excessive irritation develops. Avoid getting into the eyes or on mucous membranes. Avoid inhaling this product.

Directions

• Clean the affected area.
• Apply a small amount of product on the area 1 o 3 times daily
• May be covered with a sterile bandage.
• If bandaged, let dry first.

Other Information

• Does not contain, nor is intended as a substitute for grain or ethyl alcohol
• Will produce serious gastric disturbances if taken internally

Question or comments?

Call 956 728-8899

Package Labeling:

INGREDIENTS AND APPEARANCE

ISOPROPYL ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67326-035
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: 67326-035-00	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/20/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/20/2020

Labeler - Degasa, S.A. de C.V. (812771980)

Establishment
Name	Address	ID/FEI	Business Operations
Degasa, S.A. de C.V.		812771980	manufacture(67326-035)