HAND SANITIZER- alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Lil' Drug Store Products, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active ingredient

Ethyl alcohol 62% w/w

Purpose

Antiseptic

Use

• for handwashing to decrease bacteria on the skin

Warnings

Flammable, keep away from fire or flame.

For external use only.

Do not use

• in the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

• irritation and redness develop and persists for more than 72 hours.

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

Directions

• wet hands thoroughly with product
• briskly rub hands together until dry
• supervise children in the use of this product

Other information

• store at room temperature 15° to 30°C (59° to 86°F)
• may discolor certain fabrics

Inactive ingredients

water, carbomer, fragrance, triethanolamine, glycerin, propylene glycol, isopropyl alcohol, isopropyl myristate, tocopheryl acetate, aloe vera extract

Questions or comments?

call toll-free 1-877-507-6516 (M-F 8AM-4:30PM CST)

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Distributed by: Lil' Drug Store Products, Inc.
1201 Continental Place NE, Cedar Rapids, IA 52402

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Blister Pack

QUALITY
GUARANTEED

Hand
Sanitizer

Kills 99.99% of Germs*

* Effective at eliminating 99.99% of many common
harmful germs and bacteria in as little as 15 seconds.

Lil'
Drug Store®

1 FL OZ
(30 mL)

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66715-7012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	0.62 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Trolamine (UNII: 9O3K93S3TK)
Glycerin (UNII: PDC6A3C0OX)
Propylene Glycol (UNII: 6DC9Q167V3)
Carbomer interpolymer type A (Allyl sucrose crosslinked) (UNII: 59TL3WG5CO)
isopropyl myristate (UNII: 0RE8K4LNJS)
Isopropyl Alcohol (UNII: ND2M416302)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
.Alpha.-Tocopherol (UNII: H4N855PNZ1)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66715-7012-8	1 in 1 PACKAGE	10/01/2009
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	10/01/2009

Labeler - Lil' Drug Store Products, Inc (093103646)