Label: BLACK SNAIL COLLAGEN TONER- snail secretion filtrate, collagen liquid
- NDC Code(s): 73590-0014-1
- Packager: NOKSIBCHO cosmetic Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
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
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Water
Betula Alba Juice
Butylene glycol
Methyl Gluceth-20
Sodium Hyaluronate
1,2-Hexanediol
Water
Glycoproteins
Sodium Hyaluronate
Betaine
Butylene glycol
Glycerin
1,2-Hexanediol
Viola Mandshurica Flower Extract
Morus Alba Fruit Extract
Sea Water
Galactomyces Ferment Filtrate
Portulaca Oleracea Extract
PPG-26-Buteth-26
PEG-40 Hydrogenated Castor Oil
Allantoin
Black Soybean Extract
Sesamum Indicum (Sesame)
Seed Extract
Oryza Sativa (Rice) Extract
Theobroma Cacao (Cocoa) Extract
Panax Ginseng Berry Extract
Adenosine
Copper Tripeptide-1
Hydrolyzed Collagen
Carbomer
Triethanolamine
Dipotassium Glycyrrhizate
Ethylhexylglycerin
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 COLLAGEN TONER
snail secretion filtrate, collagen liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73590-0014 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:73590-0014-1 150 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(73590-0014)