HAND SANITIZER LIL DRUG STORE PRODUCTS, INC.- 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]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Use

For handwashing to decrease bacteria on the skin.

Warnings

Flammable, keep away from fire or flame. For external use only.

Stop use and ask a doctor if irritation and redness develops or persists.

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

Wet hands with product and rub briskly until dry.

Other Information

Do not store above 100°F. May discolor some fabrics. Harmful to wood finishes and plastics.

Inactive Ingredients

Water, Triethanolamine, Glycerin, Propylene Glycol, Carbomer, Fragrance, Isopropyl Myristate, Tocopheryl Acetate, Aloe Barbadensis Gel

SPL UNCLASSIFIED SECTION

Proudly distributed by Circle K Stores Inc.

PRINCIPAL DISPLAY PANEL - 15 mL Bottle Label

K®

Instant
Hand Sanitizer
Moisturizing with
Vitamin E & Aloe

Kills 99.99% of
Harmful Germs

0.5 FL OZ (15 mL)

INGREDIENTS AND APPEARANCE

HAND SANITIZER   LIL DRUG STORE PRODUCTS, INC.
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66715-5763(NDC:64893-030)
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)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
.Alpha.-Tocopherol (UNII: H4N855PNZ1)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66715-5763-0	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/18/2015	08/10/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	11/18/2015	08/10/2020

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