PHARMACYS PRESCRIPTION HAND SANITIZER- alcohol gel

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 Ingredients

Active ingredients - Ethyl Alcohol 71.5%

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

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 - Apply as needed into your palms and thoroughly spread on both hands. - rub in skin until dry.

Other Information

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

-may discolor fabrics.

Inactive Ingredients

INACTIVE INGREDIENTS: Purified Water (Aqua), Isopropanol, Propylene Glycol, Isopropyl Myristate.

Distributed By:

Distributed By:

American Consumer Products Corp

Vernon, CA 90058

Pharmacys Prescription Hand Sanitizer

INGREDIENTS AND APPEARANCE

PHARMACYS PRESCRIPTION HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72197-024
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	71.5 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72197-024-05	117 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/17/2020

Labeler - American Consumer Products Corp (081101181)