Label: DR COSIGN CCE PREMIUM REPAIR- dimethicone, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 72642-020-01, 72642-020-02, 72642-020-03 - Packager: Naerok Resources 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 November 6, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients:
Water, Butylene Glycol, Cetearyl Alcohol, Glycerin, Corylus Avellana (Hazel) Seed Oil, Cocos Nucifera (Coconut) Oil, Glyceryl Stearate, Hydrogenated Olive Oil Decyl Esters, Citrus Grandis(Grapefruit) Peel Oil, Canola Oil,
Butyrospermum Park Ⅱ(Shea Butter), Polysorbate 60, Olivoyl Hydrolyzed Wheat Protein, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Tocopheryl Acetate, Sorbitan Stearate, Ceramide 3, Citric Acid, Isohexadecane, Glyceryl Oleate, Scutellaria Baicalensis Root Extract, Paeonia Suffruticosa Root Extract, Polysorbate 80, Caprylyl Glycol, Allantoin, Boswellia Serrata Resin Extract, Xanthan Gum, Sorbitan Oleate, Tremella Fuciformis Sporocarp Extract, Cammellia Sinensis Leaf Extract, Morus Alba Root Extract, Origanum Vulgare Leaf Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Centella Asiatica Extract, 1,2-Hexanediol, Disodium EDTA, Potassium Sorbate, Sodium Benzoate, Fragrance, Lactobacillus - PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL-50mL Carton
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL - 20mL Tube
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INGREDIENTS AND APPEARANCE
DR COSIGN CCE PREMIUM REPAIR
dimethicone, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72642-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Dimethicone (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) Dimethicone 3.0 g in 100 mL Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.04 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:72642-020-02 1 in 1 CARTON 10/01/2018 1 NDC:72642-020-01 50 mL in 1 CONTAINER; Type 0: Not a Combination Product 2 NDC:72642-020-03 20 mL in 1 TUBE; Type 0: Not a Combination Product 10/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/01/2018 Labeler - Naerok Resources Co., Ltd (694203684) Registrant - Naerok Resources Co., Ltd (694203684) Establishment Name Address ID/FEI Business Operations Naerok Resources Co., Ltd 694203684 manufacture(72642-020)