PREVENT RUBBING ALCOHOL ISOPROPYL 70 PERCENT- isopropyl alcohol liquid

Prevent Rubbing Alcohol Isopropyl 70 Percent by

Drug Labeling and Warnings

Prevent Rubbing Alcohol Isopropyl 70 Percent by is a Otc medication manufactured, distributed, or labeled by Eco-Med Pharmaceuticals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

ACTIVE INGREDIENT

Isopropyl alcohol (70% v/v conc.)

PURPOSE:

First Aid Antiseptic

USES:

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

WARNINGS:

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

Flammable, keep away from fire or flame. Use only in a well-ventillated 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.

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.

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 substitute for grain or ethyl alcohol.

INACTIVE INGREDIENT:

Purified water.

Questions:

1-844-432-6633 Mon- Fri 8am - 4 pm (EST) Email: info@eco-med.com

Package Labeling:

INGREDIENTS AND APPEARANCE

PREVENT RUBBING ALCOHOL ISOPROPYL 70 PERCENT 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78835-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 mL  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78835-006-01	12 in 1 BOX	10/26/2020
1		500 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/26/2020

Labeler - Eco-Med Pharmaceuticals, Inc. (249183435)