PHARMACYS PRESCRIPTION HAND SANITIZER- alcohol spray

Pharmacys Prescription Hand Sanitizer by

Drug Labeling and Warnings

Pharmacys Prescription Hand Sanitizer 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 ingredients - Ethyl Alcohol 80%

Purpose

Purpose: Antiseptic

Warnings

Warnings - For external use only. Do not swallow.

Flammable. Keep away from fire or flame.

Do not apply around eyes. Do not use in ears & mouth.

Indications & Usage Section

When using this product, avoid contact with eyes.

In case of contact, flush eyes with water.

Stop Use

Stop use and ask a doctor if redness or irritation develops and persists for more than 72 hours.

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.

Directions

Directions - Spray directly onto hands, rub into skin until dry. Spray directly onto surfaces: knobs, handles, steering wheels, light switches, grocery carts, countertops, etc and let dry.

Other Information

Other information - store at 20°C (68° to 77 F°).

- may discolor fabrics.

Inactive Ingredients

INACTIVE INGREDIENTS: Purified Water (Aqua), Glycerin, Hydrogen Peroxide.

Distributed By

Distributed By:

American Consumer Products Corp

Vernon, CA 90058

Pharmacys Prescription Hand Sanitizer

INGREDIENTS AND APPEARANCE

PHARMACYS PRESCRIPTION HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72197-023
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72197-023-05	147 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/16/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/16/2020

Labeler - American Consumer Products Corp (081101181)