ISOPROPYL ALCOHOL liquid

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredient

Isopropyl alcohol (70%conc)

Purpose

First aid antiseptic

Warnings

For external use only.

-if taken internally, serious gastric disturbances will result

Flammable keep away from fire or flamme

-use only in a 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 one week unless directed by a doctor

Stop use and ask a doctor if

condition persists or gets worse

keep out of reach of children

In case of ingestion, get medical help or contact a Poison Control Center right away (1-800-222-1222)

Directions

-clean affected area

-apply small amount of this product on the area 1-3 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 subsitute for grain or ethyl alcohol

Inactive ingredient

purified water

Directions

-clean affected area

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

-if bandaged, let dry first

-may be covered with a sterile bandage

PRINCIPAL DISPLAY PANEL

Bioliving

70% isopropyl alcohol

warning flammable

keep away from heat, spark, electrical, fire or flamme

use only in a well-ventilated area; fumes may be harmful

32FL OZ (1QT) 946 mL

INGREDIENTS AND APPEARANCE

ISOPROPYL ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83123-0019
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	30 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83123-0019-1	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/17/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/17/2023

Labeler - BROSANT GROUP LLC (117037683)