99.9% ISOPROPYL ALCOHOL solution

99.9% Isopropyl Alcohol by

Drug Labeling and Warnings

99.9% Isopropyl Alcohol by is a Otc medication manufactured, distributed, or labeled by Belle Chemical LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Isopropyl alcohol 99.9%

PURPOSE

First Aid Antiseptic

WARNINGS

For external use only. If taken internally serious gastric disturbances will result.

Flammable keep away from fire or flame, heat, spark, electrical.

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.

ASK DOCTOR

Ask a doctor before use for deep or puncture wounds, animal bites or serious burns

WHEN USING

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

Stop use and ask doctor if condition persists or gets worse

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions

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

INDICATIONS & USAGE

helps prevent the risk of infection in:

• minor cuts
• scrapes
• burns

SPL UNCLASSIFIED SECTION

Other information:

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

INACTIVE INGREDIENT

Water

QUESTIONS

Questions and Comments:

www.bellechemical.com

877-522-2233

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

99.9% ISOPROPYL ALCOHOL 
99.9% isopropyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82771-999
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	999 mL  in 1000 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82771-999-32	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/24/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/24/2022

Labeler - Belle Chemical LLC (060891550)