PHARMACYS PRESCRIPTION IPA WINTERGREEN- isopropyl alcohol liquid

Pharmacys Prescription IPA Wintergreen by

Drug Labeling and Warnings

Pharmacys Prescription IPA Wintergreen by is a Otc medication manufactured, distributed, or labeled by American Consumer Products Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient (by volume)

Isopropyl alcohol (70% conc.)

Purpose

Purpose

First Aid Antiseptic

Uses

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

Warnings

Warnings

For external use only

If taken internally serious gastric disturbances will result

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

When using this product

When using this product do not get into eyes do not inhale do not apply over large area of the body do not use longer than 1 week

Stop use

Stop use and ask a 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.

Caution

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 eyes or mucus membranes. Avoid inhaling this product.

Directions

Directions clean the affected area apply a small amount of this product on the area 1 to 2 times daily may be covered with a sterile bandage if bandaged, let dry first

Other information

Other information does not contain, nor is intended as a substitute for grain or ethyl alcohol.

Inactive ingredient

Inactive ingredient Water (Aqua), Methyl Salicylate, FD&C Blue #1, FD&C Yellow #5

Tamper Evident

Tamper Evident: Do Not Use if the under cap safety foil is broken or missing.

Distributed by

Distributed by:

American Consumer Products Corp

Vernon, CA 90058

Principal Display Panel

INGREDIENTS AND APPEARANCE

PHARMACYS PRESCRIPTION IPA WINTERGREEN 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72197-037
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
METHYL SALICYLATE (UNII: LAV5U5022Y)
WATER (UNII: 059QF0KO0R)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72197-037-12	354.8 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/14/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/14/2020

Labeler - American Consumer Products Corp (081101181)