LIQUID HAND CLEANSE- triclosan gel

Liquid Hand Cleanse by

Drug Labeling and Warnings

Liquid Hand Cleanse by is a Otc medication manufactured, distributed, or labeled by Great Lakes Wholesale & Marketing, LLC, China Ningbo Shangge Cosmetic Technology Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                 Purpose

Triclosan 0.2%......................Antiseptic

PURPOSE

Health Care Instant Hand Sanitizer - Ice Clear - Extra Enriched with Vitamin E Bead & Aloe

Kills 99.9% of Germs without water or towels!

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.

INDICATIONS & USAGE

USE: 

• handwashing to decrease bacteria on the skin

WARNINGS

Warnings:

for external use only.

Flammable. Keep away from heat and flame.

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 persist for more than 72 hours.

DOSAGE & ADMINISTRATION

Directions:

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

INACTIVE INGREDIENT

Inactive ingredients:

aloe vera leaf juice, carbomer, glycerin, propylene glycol, tocopheryl acetate (vitamin E), triethanolamine, water.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LIQUID HAND CLEANSE 
triclosan gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64092-316
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	10 mg  in 500 mg

Inactive Ingredients
Ingredient Name	Strength
CETETH-7 (UNII: 4ST6952Q67)
ETHYL SULFATE (UNII: P3LK0HF3B7)
COCONUT OIL (UNII: Q9L0O73W7L)
DIETHANOLAMINE (UNII: AZE05TDV2V)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
OCTHILINONE (UNII: 4LFS24GD0V)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EDETATE DISODIUM (UNII: 7FLD91C86K)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 40 (UNII: WZB9127XOA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64092-316-01	500 mg in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/05/2013

Labeler - Great Lakes Wholesale & Marketing, LLC (361925498)

Establishment
Name	Address	ID/FEI	Business Operations
China Ningbo Shangge Cosmetic Technology Corp.		529287434	manufacture(64092-316)