70% ISOPROPYL RUBBING ALCOHOL solution

70% Isopropyl Rubbing Alcohol by

Drug Labeling and Warnings

70% Isopropyl Rubbing Alcohol by is a Otc medication manufactured, distributed, or labeled by Belle Chemical LLC, Belle Chemical. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Isopropyl Alcohol 70%

ASK DOCTOR

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

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.

PURPOSE

helps prevent the risk of infection in: minor cuts, scrapes, and 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

QUESTIONS

Questions and Comments: www.bellechemical.com; 877-522-2233

DOSAGE & ADMINISTRATION

• 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

WARNINGS

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

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

INACTIVE INGREDIENT

Water

INDICATIONS & USAGE

helps prevent the risk of infection in:

• minor cuts
• scrapes
• burns

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

70% ISOPROPYL RUBBING ALCOHOL 
70% isopropyl rubbing alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82771-070
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	1 mL  in 700 mg

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82771-070-32	700 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/17/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/17/2022	11/14/2025

Labeler - Belle Chemical LLC (060891550)

Registrant - Belle Chemical LLC (060891550)

Establishment
Name	Address	ID/FEI	Business Operations
Belle Chemical		060891550	manufacture(82771-070)