GET CLEAN MOISTURIZING HAND SANITIZER- alcohol gel

Get Clean Moisturizing Hand Sanitizer by

Drug Labeling and Warnings

Get Clean Moisturizing Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Shaklee Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Alcohol 65%. Purpose: Antiseptic

INDICATIONS & USAGE

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use wehn soap and water are not available.

WARNINGS

For external use only. Flamable. Keep away from heat or flame.

DO NOT USE

• On children less than 2 months of age
• On open skin wounds

WHEN USING

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

STOP USE

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

ASK DOCTOR

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• 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.

Other Information

• Store between 15-30°C (59-86°F).
• Avoid freezing and excessive heat above 40°C (104°F)

INACTIVE INGREDIENT

Water, Glycerine, Squalane, Acrylates Copolymer, Sodium Hydroxide

Questions of Comments

Call 1-800-426-0766

PURPOSE

Hand sanitizer to help reduct bacteria that potentially can cause disease. For use when soap and water are not available.

DOSAGE & ADMINISTRATION

Place enough product on hands to cover all surfaces. Rub hands together until dry.

PRINCIPAL DISPLAY PANEL

237 mL NDC: 59899-050-01

INGREDIENTS AND APPEARANCE

GET CLEAN MOISTURIZING HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59899-050
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SQUALANE (UNII: GW89575KF9)
ETHYL ACRYLATE (UNII: 71E6178C9T)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59899-050-01	237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/18/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/18/2020

Labeler - Shaklee Corporation (020284076)