BELLASKIN BRIGHTENING CONTOUR ESSENCE- niacinamide cream
Ajou Medics Co., Ltd

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Drug Facts

active ingredient: niacinamide

inactive ingredient: Water, Glycerin, Butylene Glycol, Beta-Glucan, Cetanol, Caprylic / Capric Triglyceride, Squalane, Cucubita Pepo(Pumpkin) Fruit Extract, Murdania Keisak Extract, Hamamelis Virginiana(Witchhazel) Leaf Extract, Glyceryl Stearate/ PEG-100 Stearate, Dimethicone, Polysorbate-60, Glyceryl Stearate, Collagen, Beeswax, Methyl Paraben, Phenoxy Ethanol, Arginine, Carbomer, Sorbitan Stearate, Allantoin, Fragrance, Ceramide 3, Propyl Paraben, Acetyl Hexapeptide-8, Copper Tripeptide-1,
Dipotassium Glycyrrhizate, Xanthan gum, Tocopheryl Acetate, Sodium Hyaluronate

whitening and brightening the skin

keep out of reach of the children

Apply Proper Amount of the essence on the face

■ For external use only.
■ Avoid contact with eyes.
■ Do not swallow. If swallowed, get medical help.
■ Keep out of reach of children.
■ Stop use and ask doctor if rash and irritation develops.

wash the skin to be applied

BELLASKIN BRIGHTENING CONTOUR ESSENCE
niacinamide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76340-0007
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	2 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SQUALANE (UNII: GW89575KF9)
PUMPKIN (UNII: SYW0QUB89Y)
HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
DIMETHICONE (UNII: 92RU3N3Y1O)
POLYSORBATE 60 (UNII: CAL22UVI4M)
COLLAGENASE (UNII: 9X7O8V25IT)
METHYLPARABEN (UNII: A2I8C7HI9T)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:76340-0007-1	40 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	01/01/2016	04/18/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		09/13/2011	04/18/2022

Labeler - Ajou Medics Co., Ltd (688796473)

Registrant - Ajou Medics Co., Ltd (688796473)

Name	Address	ID/FEI	Business Operations
Establishment
Ajou Medics Co., Ltd		688796473	manufacture(76340-0007)

Revised: 4/2022

Document Id: dce5027f-2844-091d-e053-2995a90a5a7b

Set id: 672012ea-8807-6da5-e053-2991aa0ac322

Version: 2

Effective Time: 20220417

Ajou Medics Co., Ltd