HYDRO ALCOHOL GEL- alcohol gel

Hydro Alcohol Gel by

Drug Labeling and Warnings

Hydro Alcohol Gel by is a Otc medication manufactured, distributed, or labeled by BRENNTAG MID-SOUTH, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Purpose

Antiseptic

Use(s)

WARNING

KEEP OUT OF REACH OF CHILDREN

Inactive ingredients

STORAGE

DIRECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

HYDRO ALCOHOL GEL HAND RUB

INGREDIENTS AND APPEARANCE

HYDRO ALCOHOL GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65353-3291
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	73.3 L  in 100 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	23.1 L  in 100 L
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)	1.1 L  in 100 L
GLYCERIN (UNII: PDC6A3C0OX)	2.5 L  in 100 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65353-3291-1	2600 L in 1 TANK; Type 0: Not a Combination Product	04/01/2020
2	NDC: 65353-3291-2	208 L in 1 DRUM; Type 0: Not a Combination Product	04/01/2020
3	NDC: 65353-3291-3	1040 L in 1 TANK; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/01/2020

Labeler - BRENNTAG MID-SOUTH, INC. (122625064)

Registrant - BRENNTAG MID-SOUTH, INC. (122625064)