BANOBAGI MILK THISTLE REPAIR- niacinamide, adenosine, glycerin cream

Banobagi Milk Thistle Repair by

Drug Labeling and Warnings

Banobagi Milk Thistle Repair by is a Otc medication manufactured, distributed, or labeled by Banobagi Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

niacinamide, adenosine

INACTIVE INGREDIENT

Arctium Lappa Root Extract, Caprylic/Capric Triglyceride, Glycerin, 1,2-Hexanediol, Hydrogenated Polydecene, Caprylyl Methicone, Vinyl Dimethicone, Dipropylene Glycol, Silybum Marianum Seed Extract, Cetyl Ethylhexanoate, Cetearyl Alcohol, Niacinamide, Cetearyl Olivate, Glyceryl Stearate, Sorbitan Olivate, Squalane, Panthenol, Helianthus Annuus (Sunflower) Seed Oil Unsaponifiables, Copper Tripeptide-1, Madecassoside, Cardiospermum Halicacabum Flower/Leaf/Vine Extract, Echium Plantagineum Seed Oil, Sodium Hyaluronate, Adenosine, Stearic Acid, Ammonium Acryloyldimethyltaurate/VP Copolymer, Polyglyceryl-2 Stearate, Hydroxyacetophenone, Octyldodecanol, Stearyl Alcohol, Sodium Polyacryloyldimethyl Taurate, Dimethiconol, Hydrogenated Lecithin, Caprylyl/Capryl Glucoside, Xanthan Gum, Disodium EDTA, Glyceryl Acrylate/Acrylic Acid Copolymer, Ethylhexylglycerin, Tocopherol

PURPOSE

Brightening, , Anti-wrinkle, Repair, Recovery

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

After cleansing or at the last step of your skin care, use several drops and spread around evenly on your face and gently pat to absorb the cream

WARNINGS

1. If abnormal symptoms or side effects such as red spots, swelling, or itching are present in the cosmetics or in the direct sunlight after use, consult a specialist

2. Do not use in wounded areas

3. Precautions for storage and handling

- Keep out of reach of children

- Keep away from direct sunlight

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BANOBAGI MILK THISTLE REPAIR 
niacinamide, adenosine, glycerin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72001-0017
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	2 g  in 100 mL
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	ADENOSINE	0.04 g  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	5 g  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72001-0017-1	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/28/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part347	01/28/2019

Labeler - Banobagi Co., Ltd. (694436539)

Registrant - Banobagi Co., Ltd. (694436539)

Establishment
Name	Address	ID/FEI	Business Operations
DERMAMEAL CO., LTD.		694253327	manufacture(72001-0017)

Establishment
Name	Address	ID/FEI	Business Operations
Banobagi Co., Ltd.		694436539	label(72001-0017)