LANBELLE EGF FGF AMPULE- glycerin liquid

LANBELLE EGF FGF Ampule by

Drug Labeling and Warnings

LANBELLE EGF FGF Ampule by is a Otc medication manufactured, distributed, or labeled by TAMLATAMANU Inc., Choice Cosmetic Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Glycerin

INACTIVE INGREDIENT

Centella Asiatica Extract, Sodium Hyaluronate

PURPOSE

Skin Balancing

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

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

INDICATIONS & USAGE

After using clear toner, take a drop in the forehead and the cheeks in the morning and the evening.

It can be used in combination with LANBELLE hydrating duo serum.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LANBELLE EGF FGF AMPULE 
glycerin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72084-0005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CENTELLA ASIATICA (UNII: 7M867G6T1U)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72084-0005-1	15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	03/27/2018

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
Choice Cosmetic Co., Ltd.		688197261	label(72084-0005) , manufacture(72084-0005) , pack(72084-0005)

Establishment
Name	Address	ID/FEI	Business Operations
TAMLATAMANU Inc.		694763633	relabel(72084-0005)