DR DEEP BRIGHTENING FACIALEMULSION- allantoin emulsion

Dr Deep Brightening FacialEmulsion by

Drug Labeling and Warnings

Dr Deep Brightening FacialEmulsion by is a Other medication manufactured, distributed, or labeled by MineralHouse Corporation, Bobo Cosmetic Co.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Allantoin 0.2%

PURPOSE

Purpose: Skin Protectant

WARNINGS

Warnings:

- For external use only

- Do not use on wounds or damaged skin

WHEN USING

When using this product, do not use other than directed

STOP USE

Stop use if allergic reaction or irritation occurs

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

- If swallowed, get medical help or contact a Poison Control Center immediately

STORAGE AND HANDLING

Storage: Keep in a dry and cool place

INSTRUCTIONS FOR USE

Adults and children over 6 years old:

- Step1: Clean and dry the face or the body

- Step2: Spread a proper amount thoroughly to the face or the body

Children under 6 years old: Consult your medical professional

INACTIVE INGREDIENT

Inactive Ingredients: Water, Cyclopentasiloxane, Glycerin, Arbutin, Sodium Hyaluronate, Cyclomethicone, Citrus Paradisi (Grapefruit) Seed Extract, Dimethicone, Dimethicone/Vinyl Dimethicone Crosspolymer, Olea Europaea (Olive) Fruit Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Tocopheryl Acetate, Silk Extract, Aloe Barbadensis Leaf Juice Powder, Sorbitan Sesquioleate, Camelia Sinensis Leaf Extract, Magnolia Kobus Bark Extract, Propolis Extract, Salix Alba (Willow) Bark Extract

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR DEEP BRIGHTENING FACIALEMULSION 
allantoin emulsion

Product Information
Product Type	COSMETIC	Item Code (Source)	76015-910
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.24 g  in 120 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ARBUTIN (UNII: C5INA23HXF)
CYCLOMETHICONE (UNII: NMQ347994Z)
CITRUS PARADISI SEED (UNII: 12F08874Y7)
DIMETHICONE (UNII: 92RU3N3Y1O)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
OLEA EUROPAEA FRUIT VOLATILE OIL (UNII: 8E7358CX1J)
SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17)
MAGNOLIA KOBUS BARK (UNII: 54LVP49595)
PROPOLIS WAX (UNII: 6Y8XYV2NOF)
SALIX ALBA BARK (UNII: 205MXS71H7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	76015-910-01	120 mL in 1 BOTTLE, DISPENSING

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	04/10/2015

Labeler - MineralHouse Corporation (557802539)

Registrant - MineralHouse Corporation (557802539)

Establishment
Name	Address	ID/FEI	Business Operations
MineralHouse Corporation		557802539	relabel, repack

Establishment
Name	Address	ID/FEI	Business Operations
Bobo Cosmetic Co.		669778744	manufacture