CLEARGUARD HAND SANITIZER- alcohol solution

ClearGuard Hand Sanitizer by

Drug Labeling and Warnings

ClearGuard Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by EVP International, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

ACTIVE INGREDIENT

Active ingredient

Alcohol 70% v/v

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Uses

to help reduce bacteria on skin

WARNINGS

Warnings

For external use only

Flammable, keep away from heat or flame.

When using this product keep away from eyes. In case of eye contact, rinse eyes with water.

Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

Keep out of reach of children. If swallowed, get medial help or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION

Directions

• apply liberally to hands to cover all surfaces
• rub hands together until dry
• supervise children under 6 years old
• not recommended for infants

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Other information

• store between 15-30°C (59-86°F)

INACTIVE INGREDIENT

Inactive ingredients

glycerin, hydrogen peroxide, purified water, acrylates/C10-30 alkyl acrylate crosspolymer, aminomethyl propanol, lauryl lactate, fragrance

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Distributed by LumAware

Cincinnati, OH 45219

Questions? Call 513-761-7614

PRINCIPAL DISPLAY PANEL

ClearGuard

Hand Sanitizer

Alcohol Based

2 FL OZ (59 mL)

INGREDIENTS AND APPEARANCE

CLEARGUARD HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80996-002
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
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
LAURYL LACTATE (UNII: G5SU0BFK7O)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80996-002-02	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/01/2021

Labeler - EVP International, LLC (965692812)