PHARMACYS PRESCRIPTION HAND SANITIZER- alcohol liquid

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 75%

Purpose

Purpose: Antiseptic

Uses - Reduces bacteria on skin that could cause disease.

Warnings

Warnings - For external use only. Do not ingest or swallow.

Flammable. Keep away from fire or flame.

Stop Use

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

Keep out of reach of children

Keep out of reach of children. Do not use on children less than 2 months of age. If swallowed, get medical help or contact a Poison Control Center right away.

Inactive Ingredients

Inactive ingredients - Glycerin, propylene glycol, triethanolamine, carbomer, fragrance, disodium edta, tocopheryl acetate, deionized water.

Directions

Directions: apply as needed in your palms, rub into skin until dry.

Indications & Usage Section

When using this product, avoid contact with eyes. In case of contact, flush eyes with water.

Pharmacy's Prescription Label

INGREDIENTS AND APPEARANCE

PHARMACYS PRESCRIPTION HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72197-035
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL 2-(2-METHYLBUTYRATE) (UNII: 3Z73C506A9)
CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
TRIETHANOLAMINE 2-CYCLOHEXYL-4,6-DINITROPHENOLATE (UNII: N2TK31JIAH)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72197-035-10	10 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/15/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/15/2021

Labeler - American Consumer Products Corp (081101181)