BIOMAX USA- isopropyl alcohol liquid

Biomax USA by

Drug Labeling and Warnings

Biomax USA by is a Otc medication manufactured, distributed, or labeled by Biomax Cosmetics. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

ACTIVE INGREDIENT

Active Ingredient: 70% Isopropyl Alcohol

PURPOSE

Purpose: Antiseptic

USES

hand sanitizer to decrease bacteria on the skin

recommended for repeated use

for use when soap and water are not available

INACTIVE INGREDIENT

Inactive Ingredients: Purified Water/aqua

WARNINGS

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

Flammable - keep away from heat, spark, electrical, fire or flame. Ask a doctor before use for 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.

DIRECTIONS

supervise children under 6 years of age when using this product to avoid swallowing

SPL UNCLASSIFIED SECTION

HEALTHCARE

ISOPROPYL RUBBING ALCOHOL 70%

WARNING: FLAMMABLE,

KEEP AWAY FROM FIRE OR FLAME

ANTISEPTIC

Topical antiseptic and sanitizer

Antibacterial Cleansing Agent

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.

Biomax Cosmetics Inc.

Houston, TX 77061

www.biomaxcosmetics.com

MADE IN USA

Packaging

INGREDIENTS AND APPEARANCE

BIOMAX USA 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77369-899
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77369-899-16	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/05/2020
2	NDC: 77369-899-01	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/05/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/05/2020

Labeler - Biomax Cosmetics (084032031)

Establishment
Name	Address	ID/FEI	Business Operations
Biomax Cosmetics		084032031	manufacture(77369-899)