Clere Hand Sanitizer - 13.5oz (gel) NDC: 76894-0003-1

Clere Hand Sanitizer by

Drug Labeling and Warnings

Clere Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by M&M Products. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CLERE HAND SANITIZER- ethyl alcohol gel 
M&M Products

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Clere Hand Sanitizer - 13.5oz (gel) NDC: 76894-0003-1

Active Ingredient(s)

Ethyl Alcohol 70%

Purpose

Antimicrobial

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. Recommended for repeated use.

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 do not use in or near the eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

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

Directions

Place enough product in your palm to thoroughly cover your hands

Rub hands together briskly until dry

Children should be supervised when using product

Other information

Do not store above 110F (43C)

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, Glycerin, Isopropyl Myristate, Propylene Glycol, Tocopheryl Acetate, Aminomethyl Propanol, Carbomer.

Questions or comments?

Call 1-800-707-8763

Monday to Friday 8:30AM to 5:00PM

Package Label - Principal Display Panel

DISTRIBUTED BY:

M&M Products Company

Marietta, GA 30067 USA

Made in South Africa

www.mmproducts.com

Clere Hand Sanitizer (gel) - 13.5 oz (400 mL) NDC: 76894-0003-1

CLERE HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76894-0003
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76894-0003-1	400 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/27/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/27/2020	11/03/2021

Labeler - M&M Products (837913276)

Revised: 11/2021

Document Id: cfe763c1-982b-3d3e-e053-2995a90a5763

34390-5

Set id: ade2e280-2393-ee0d-e053-2995a90adc62

Version: 3

Effective Time: 20211103