LANBELLE WHITENING GELMASKPACK GRAPEFRUIT THERAPY- glycerin liquid

LANBELLE WHITENING GELMASKPACK GRAPEFRUIT THERAPY by

Drug Labeling and Warnings

LANBELLE WHITENING GELMASKPACK GRAPEFRUIT THERAPY by is a Otc medication manufactured, distributed, or labeled by TAMLATAMANU Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Glycerin

INACTIVE INGREDIENT

Water, Niacinamide, etc.

PURPOSE

Skin protectant

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

After washing your face, prepare the skin with toner.
Spread the sheet mask evenly over the face.
Leave it for 5-10 minutes and remove the mask.
Gently pat until fully absorbed.

WARNINGS

1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LANBELLE WHITENING GELMASKPACK GRAPEFRUIT THERAPY 
glycerin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72084-0012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	8 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
NIACINAMIDE (UNII: 25X51I8RD4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72084-0012-1	10 in 1 PACKAGE	03/27/2018
1		25 g 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 not final	part347	03/27/2018

Labeler - TAMLATAMANU Inc. (694763633)

Registrant - TAMLATAMANU Inc. (694763633)

Establishment
Name	Address	ID/FEI	Business Operations
TAMLATAMANU Inc.		694763633	pack(72084-0012) , manufacture(72084-0012) , label(72084-0012)