Label: DR CELLINME MASK SHEET- niacinamide patch
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Contains inactivated NDC Code(s)
NDC Code(s): 69783-020-01 - Packager: Dr.Gene 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 July 28, 2015
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredients: Water, Glycerin, Butylene Glycol, 1,2-Hexanediol, Biosaccharide Gum-1, PEG-60 Hydrogenated Castor Oil, Soy Isoflavones, Chamomilla Recutita (Matricaria) Flower Extract, Centella Asiatica Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Butylene Glycol, Arginine, Hydrolyzed Collagen, Allantoin, Carbomer, Xanthan Gum, Hydroxyethylcellulose, Adenosine, Dipotassium Glycyrrhizate, Panthenol, Human Oliqopeptide - 1
- PURPOSE
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WARNINGS
Warnings: 1. You must immediately discontinue using the product if any of the following symptoms occur, and since a prolonged usage will aggressive the symptoms, you must consult with a doctor specializing in dermatology. A. If abnormal symptoms such as red spots, swelling, itchiness and/or irritation occur. B. If the applied experience the above symptoms due to direct sunlight. 2. Do not use on areas with various wounds, eczema and/or dermatitis those who are sensitive to adhesive band-aids or poultice must take caution when using it. Keep away from your eyes and be sure to clean it immediately if it ever gets into an eye. 3. Safety cautions in storage and handling. A. Use immediately after you open the product. B. Do not store in high or low temperature locations and areas exposed to direct sunlight. C. Do not reuse a product that has already been used before. Keep out of reach of children. Keep away from the hands of infants and children.
- KEEP OUT OF REACH OF CHILDREN
- How to use
- DOSAGE & ADMINISTRATION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR CELLINME MASK SHEET
niacinamide patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69783-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 0.6 mg in 5 Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69783-020-01 5 in 1 CARTON; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/01/2015 Labeler - Dr.Gene Co.,Ltd (688460085) Registrant - Dr.Gene Co.,Ltd (688460085) Establishment Name Address ID/FEI Business Operations Dr.Gene Co.,Ltd 688460085 manufacture(69783-020)
