DR.S CLEAN HAND- alcohol gel

Dr.s Clean Hand by

Drug Labeling and Warnings

Dr.s Clean Hand by is a Otc medication manufactured, distributed, or labeled by EQMAXON Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: Ethyl Alcohol 70.0%

INACTIVE INGREDIENT

Inactive ingredients:

Purified Water, Aloe Extract, Glycerin, Sodium Hyaluronate, Carbomer, Butylene Glycol, Triethanolamine, Flavor

PURPOSE

Purpose: ANTISEPTIC

WARNINGS

Warnings:

Flammable. Keep away from fire and flames. For external use only.
When using this product Do not get into eyes. If contact occurs, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or redness develops.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

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

Uses

Uses:
for hand-washing to decrease bacteria on the skin, only when water is not available

Directions

Directions:

Wet hands thoroughly with product and allow to dry without wiping

For children under 6, use only under adult supervision.

PACKAGE LABEL - Dr.'s Clean Hand Gel 60mL

PACKAGE LABEL - Dr.'s Clean Hand Gel 500mL

INGREDIENTS AND APPEARANCE

DR.S CLEAN HAND 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55526-0010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
ALOE (UNII: V5VD430YW9)
Glycerin (UNII: PDC6A3C0OX)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
Butylene Glycol (UNII: 3XUS85K0RA)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55526-0010-1	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2020
2	NDC: 55526-0010-2	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/01/2020

Labeler - EQMAXON Corp (557821534)

Registrant - EQMAXON Corp (557821534)

Establishment
Name	Address	ID/FEI	Business Operations
EQMAXON Corp		557821534	manufacture(55526-0010)