Label: DR COSIGN CCE SOOTHING RECOVERY SERUM- dimethicone, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 72642-030-01, 72642-030-02, 72642-030-03 - 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, Glycerin, Butylene Glycol, Betaine, SD Alcohol 40-B, PEG-60 Hydrogenated Castor Oil, Cocos Nucifera (Coconut) Oil, Scutellaria Baicalensis Root Extract, Paeonia Suffruticosa Root Extract, Sodium Polyacrylate, Octyldodeceth-16, Carbomer, Glyceryl Acrylate/Acrylic Acid Copolymer, Arginine, Xanthan Gum, Tremella Fuciformis Sporocarp Extract, Hamamelis Virginiana (Witch Hazel) Leaf Extract, Beta-Glucan, Rosmarinus Officinalis (Rosemary) Leaf Extract, Origanum Vulgare Leaf Extract, Centella Asiatica Extract, 1,2-Hexanediol, Disodium EDTA, Fragrance,Lactobacillus
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL - 30mL Carton
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL - 10mL Tube
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INGREDIENTS AND APPEARANCE
DR COSIGN CCE SOOTHING RECOVERY SERUM
dimethicone, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72642-030 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) Glycerin (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72642-030-02 1 in 1 CARTON 10/01/2018 1 NDC:72642-030-01 30 mL in 1 CONTAINER; Type 0: Not a Combination Product 2 NDC:72642-030-03 10 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(72642-030)
