GENE 16 WHITENING FACTOR- allantoin tablet, soluble

Gene 16 Whitening Factor by

Drug Labeling and Warnings

Gene 16 Whitening Factor by is a Otc medication manufactured, distributed, or labeled by Shanghai Liang Liang International Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Allantoin 0.5%

Purpose

Allantoin    Skin Lightener

                 Skin Protectant

Warning

For External Use Only.

Use

Apply moderate amount of the product on the skin.

Stop Using the Product if

Stop using the product when you have skin problems or the product disagrees with your skin.
・Stop using the product immediately and consult a dermatologist if you have redness, swelling, itching or irritation on the skin while or after using the product.
・If the product gets into the eyes, don't rub but rinse with water.

Keep Out of Reach of Children

Keep out of reach of children.

When Using the Product

Mix one tablet with water in palm to dissolve before applying to skin. Two tablets two times a day. One after face cleanse in the morning; and one before bed.

Other Information

Keep in a dry, cool place away from direct sunlight. Store at room temperature.

Contact the Manufacturer or Distributor

Manufactured by Shanghai Liang Liang International Inc.
No. 876, TaoGan Road, Sheshan Town, Songjiang District, Shanghai 201602, China
(86)21-57794082

Distributed by Shanghai Liang Liang International Inc (USA)

Inactive Ingredients

HYALURONIC ACID, TREHALOSE, MANNITOL, GLYCYRRHIZA GLABRA, CENTELLA ASIATICA, RESVERATROL, ARBUTIN, NIACINAMIDE, LECITHIN SOYBEAN, CERAMIDE 3, TOCOPHEROL, ASTAXANTHIN, PUNICA GRANATUM WHOLE

Drug Facts

INGREDIENTS AND APPEARANCE

GENE 16 WHITENING FACTOR 
allantoin tablet, soluble

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69764-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.5 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
HYALURONIC ACID (UNII: S270N0TRQY)
TREHALOSE (UNII: B8WCK70T7I)
MANNITOL (UNII: 3OWL53L36A)
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
RESVERATROL (UNII: Q369O8926L)
ARBUTIN (UNII: C5INA23HXF)
NIACINAMIDE (UNII: 25X51I8RD4)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
CERAMIDE 3 (UNII: 4370DF050B)
TOCOPHEROL (UNII: R0ZB2556P8)
ASTAXANTHIN (UNII: 8XPW32PR7I)
PUNICA GRANATUM WHOLE (UNII: O2ZTS50U5E)

Product Characteristics
Color	white	Score	no score
Shape	OVAL	Size	8mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69764-001-10	1 in 1 PACKAGE	09/25/2014
1		7 mg in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	09/25/2014

Labeler - Shanghai Liang Liang International Inc (547834726)

Registrant - Shanghai Liang Liang International Inc (547834726)

Establishment
Name	Address	ID/FEI	Business Operations
Shanghai Liang Liang International Inc		547834726	manufacture(69764-001)