CLAPIEL HYALON SERUM- hyaluronate sodium, niacinamide cream

Clapiel Hyalon Serum by

Drug Labeling and Warnings

Clapiel Hyalon Serum by is a Otc medication manufactured, distributed, or labeled by AUS KOREA CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Sodium Hyaluronate 35%, Niacinamide 2.0%

INACTIVE INGREDIENT

Inactive Ingredients: Water, Glycerin, Butylene Glycol, 1,2-Hexanediol, Centella Asiatica Extract, Undaria Pinnatifida Extract, Sodium Polygamma-Glutamate, Boerhavia Diffusa Root Extract, Hydrolyzed Myrtus Communis Leaf Extract, Pichia Anomala Extract, Yeast Extract, Myrothamnus Flabellifolia Callus Culture Extract, Pentylene Glycol, Lactuca Indica Extract, Corydalis Ochotensis Extract, Draba Nemorasa Extract, Chenopodium Album Flower Extract, Lactobacillus/Soybean Ferment Extract, Salix Alba Bark Extract, Cinnamomum Cassia Bark Extract, Origanum Bulgare Leaf Extract, Chamaecyparis Obtusa Leaf Extract, Portulaca Oleracea Extract, Panthenol, Carbomer, Arginine, Adenosine, Disodium EDTA

PURPOSE

Purpose: Skin Protectant

WARNINGS

Warnings: 1. In case of having following symptoms after using this, you’re advised to stop using it immediately. If you keep using it, the symptoms will get worse and need to consult a dermatologist. 1) In case of having problems such as red rash, swollenness, itching, stimulation during usage. 2) In case of having the same symptoms above on the part you put this product on by direct sunlight. 2. You are banned to use it on the part where you have a scar, eczema, or dermatitis. 3. In case of getting it into your eyes, you have to wash it immediately.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of babies and children

INDICATIONS & USAGE

Indications & Usage: Apply a desired amount evenly over entire face.

DOSAGE & ADMINISTRATION

Dosage & Administration: Take an adequate amount of this product

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CLAPIEL HYALON SERUM 
hyaluronate sodium, niacinamide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69977-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	0.6 mg  in 30 mL
HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY)	HYALURONATE SODIUM	10.5 mg  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69977-020-01	30 mL in 1 CARTON; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/01/2015

Labeler - AUS KOREA CO., LTD. (689515251)

Registrant - AUS KOREA CO., LTD. (689515251)

Establishment
Name	Address	ID/FEI	Business Operations
AUS KOREA CO., LTD.		689515251	manufacture(69977-020)