Label: BLACK SNAIL COLLAGENEMULSION- snail secretion filtrate, collagen emulsion
- NDC Code(s): 73590-0012-1
- Packager: NOKSIBCHO cosmetic Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Drug Label Information
Updated March 14, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Water
Betula Alba Juice
Butylene glycol
Sodium Hyaluronate
Glycerin
Water
Glycoproteins
Sodium Hyaluronate
Betaine
1,3 Butylene glycol
Glycerin
1,2-Hexanediol
1,2-Hexanediol
Glyceryl Acrylate/Acrylic Acid Copolymer
Propylene Glycol
Glyceryl Stearate
PEG-100 Stearate
Sea Water
Cetearyl Alcohol
Cetyl Ethylhexanoate
Isohexadecane
Galactomyces Ferment Filtrate
Viola Mandshurica Flower Extract
Morus Alba Fruit Extract
Black Soybean Extract
Sesamum Indicum (Sesame)
Seed Extract
Oryza Sativa (Rice) Extract
Panax Ginseng Berry Extract
Hydrolyzed Collagen
Adenosine
Copper Tripeptide-1
Theobroma Cacao (Cocoa) Extract
Polysorbate 60
Betaine
PEG-60 Hydrogenated Castor Oil
Sorbitan Stearate
Sodium Acrylate/Sodium AcryloyldimethylTaurate Copolymer
Isohexadecane
Polysorbate 80
Stearic Acid
Triethanolamine
Carbomer
Parfum - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
-
WARNINGS
For external use only
When using this product■ if the following symptoms occurs after use, stop use and consult with a skin specialist
red specks, swelling, itching
■ don’t use on the part where there is injury, eczema, or dermatitis
Keep out of reach of children
■ if swallowed, get medical help or contact a person control center immediately
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
BLACK SNAIL COLLAGENEMULSION
snail secretion filtrate, collagen emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73590-0012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SNAIL, UNSPECIFIED (UNII: 2VIO5GL90I) (SNAIL, UNSPECIFIED - UNII:2VIO5GL90I) SNAIL, UNSPECIFIED 60 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73590-0012-1 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/14/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/14/2020 Labeler - NOKSIBCHO cosmetic Co., Ltd. (690182175) Registrant - NOKSIBCHO cosmetic Co., Ltd. (690182175) Establishment Name Address ID/FEI Business Operations NOKSIBCHO cosmetic Co., Ltd. 690182175 manufacture(73590-0012)
