AMERIGEL HAND SANITIZER- ethyl alcohol 70% gel

Amerigel Hand Sanitizer by

Drug Labeling and Warnings

Amerigel Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Amerx Health Care Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Uses

For handwashing to decrease bacteria on skin when soap and water are not available.

Warnings

For External Use only. Flammable. Keep away from heat or flame.

Do not use

In children less than 2 months of age. On open skin wounds.

When using this product

Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

­­­­­­­­­­­­­­­­­­­Stop use and ask a doctor.

If irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

­­­­­­­­­­­­­­­­­­­­­Directions

Wet hands thoroughly with product. Rub hands together briskly until dry. Supervise children under 6 years of age when using this product.

Other Information

Store below 110F (43C)

Inactive Ingredients

Water, Aloe Barbadensis, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Propylene Glycol, PEG-8 Dimethicone, Triisopropanolamine, Linalool, FD&C Blue #1

Amerigel Hand Sanitizer

INGREDIENTS AND APPEARANCE

AMERIGEL HAND SANITIZER 
ethyl alcohol 70% gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61470-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	123.9 mL  in 177 mL

Inactive Ingredients
Ingredient Name	Strength
(C10-C30)ALKYL METHACRYLATE ESTER (UNII: XH2FQZ38D8)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
PEG-8 DIMETHICONE (UNII: GIA7T764OD)
TRIISOPROPANOLAMINE (UNII: W9EN9DLM98)
PROPYLENE GLYCOL BUTYL ETHER (UNII: 6X8776AP5Z)
LINALOOL, (+)- (UNII: F4VNO44C09)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61470-001-12	177 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2020

Labeler - Amerx Health Care Corp (836425694)

Registrant - Amerx Health Care Corp (836425694)