Label: COTTA- sodium hyaluronate, snail secretion filtrate, morus alba bark extract film, extended release
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Contains inactivated NDC Code(s)
NDC Code(s): 58748-001-01 - Packager: ECO INDUSTRY CO., LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated July 8, 2013
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INACTIVE INGREDIENT
Inactive Ingredients Water, Glycerin, Niacinamide, Caesalpinia Spinosa Gum,
Ceratonia Siliqua Gum, Peg-60 Hydrogenated Castor Oil, Dipotassium Glycyrrhizate,
Glucomannan, Tamarindus Indica Seed Gum, phenoxyethanol, Methyparaben,
Propylparaben, Disodium EDTA, Adenosinine, Tocopheryl Acetate,
Potassium Hydroxide, Fragrance
- ACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INDICATIONS & USAGE
- PURPOSE
- WARNINGS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
COTTA
sodium hyaluronate, snail secretion filtrate, morus alba bark extract film, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58748-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM .3 g in 100 g GARDEN SNAIL MUCIN (UNII: BPB1U0R467) (GARDEN SNAIL MUCIN - UNII:BPB1U0R467) GARDEN SNAIL MUCIN .1 g in 100 g MORUS ALBA ROOT BARK (UNII: SV6B76DK9N) (MORUS ALBA ROOT BARK - UNII:SV6B76DK9N) MORUS ALBA ROOT BARK .1 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) NIACINAMIDE (UNII: 25X51I8RD4) CAESALPINIA SPINOSA RESIN (UNII: WL3883U2PO) LOCUST BEAN GUM (UNII: V4716MY704) PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) KONJAC MANNAN (UNII: 36W3E5TAMG) TAMARIND SEED (UNII: 6AHP8A7OML) PHENOXYETHANOL (UNII: HIE492ZZ3T) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) EDETATE DISODIUM (UNII: 7FLD91C86K) ADENOSINE (UNII: K72T3FS567) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58748-001-01 .5 g in 1 PACKAGE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/01/2013 Labeler - ECO INDUSTRY CO., LTD (688731040) Establishment Name Address ID/FEI Business Operations ECO INDUSTRY CO., LTD 688731040 manufacture(58748-001)