ISOPROPYL ALCOHOL 99% liquid

Isopropyl Alcohol 99% by

Drug Labeling and Warnings

Isopropyl Alcohol 99% by is a Otc medication manufactured, distributed, or labeled by UBQ Industries, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Isopropyl Alcohol 99% v/v. Purpose: Antiseptic

Purpose Section

first aid antiseptic, isopropyl alcohol

Indications and usage section

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

Warnings Section

For external use only. Flammable. Keep away from heat or flame

Ask a doctor before use if you have

deep 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 using this product if

condition persists or gets worse

Keep this and all drugs our of the reach of children

In case of accidentail ingestion, seek professional assistance or contact a Poison Control Center (1-800-222-1222) immediately

Directions

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

Other information

store at room temperature. does not contain, nor is intended as a substitute for grain or ethyl alcohol. will produce serious gastric disturbances if taken internally

Inactive Ingredients

purified water

Package Label - Principal Display Panel

236 ml NDC: 80668-414-05

946.4 ml NDC: 80668-414-06

18927 ml NDC: 80668-414-01

3785 ml NDC: 80668-414-02

1892 ml NDC: 80668-414-03

473.2ml NDC: 80668-414-04

INGREDIENTS AND APPEARANCE

ISOPROPYL ALCOHOL 99% 
isopropyl alcohol 99% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80668-414
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	99 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	1 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80668-414-01	18927 mL in 1 PAIL; Type 0: Not a Combination Product	03/20/2020
2	NDC: 80668-414-02	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/20/2020
3	NDC: 80668-414-03	1892 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/20/2020
4	NDC: 80668-414-04	473.2 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/20/2020
5	NDC: 80668-414-06	946.4 mL in 1 JUG; Type 0: Not a Combination Product	03/20/2020
6	NDC: 80668-414-05	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/20/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/20/2020

Labeler - UBQ Industries, LLC (069021187)

Establishment
Name	Address	ID/FEI	Business Operations
UBQ Industries, LLC		069021187	repack(80668-414) , manufacture(80668-414) , relabel(80668-414)