Label: HONESI EXOFILA CREA M- niacinamide, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 70908-210-01, 70908-210-02 - Packager: MeFactory 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 August 30, 2018
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients: WATER,GLYCERIN,BUTYLENE GLYCOL,BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE,LIMNANTHES ALBA (MEADOWFOAM) SEED OIL,SQUALANE,HYDROGENATED VEGETABLE OIL,BUTYROSPERMUM PARKII (SHEA BUTTER),BEHENYL ALCOHOL,CETEARYL ALCOHOL,GLYCERYL STEARATE,POLYGLYCERYL-3 METHYLGLUCOSE DISTEARATE,PENTYLENE GLYCOL,HYDROGENATED LECITHIN,DIMETHICONE,STEARYL ALCOHOL,PEG-100 STEARATE,BEHENIC ACID,CARBOMER,TROMETHAMINE,PHENOXYETHANOL,CAPRYLYL GLYCOL,STEARIC ACID,XANTHAN GUM,MADECASSOSIDE,POLYPERFLUOROMETHYLISOPROPYL ETHER,MYRISTIC ACID,DISODIUM EDTA,ALTEROMONAS FERMENT EXTRACT,PROPYLENE GLYCOL,POLOXAMER 188,POLYPERFLUOROETHOXYMETHOXY DIFLUOROETHYL PEG PHOSPHATE,POTASSIUM CETYL PHOSPHATE,HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL UNSAPONIFIABLES,GLYCERYL CAPRYLATE,MACADAMIA TERNIFOLIA SEED OIL,CERAMIDE 3,PHYTOSPHINGOSINE,MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL
- PURPOSE
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WARNINGS
Warnings: 1. Discontinue use immediately and consult a dermatologist, if you experience the following: 1) Irritation, Red spots, itchy skin or rash 2) Applied skin area has the above reaction from direct sun 2. Do not use on irritated skin, cuts, or other infected skin area. 3. Avoid contact with eyes. 4. close the cap after using. 5. keep out of reach of children.
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HONESI EXOFILA CREA M
niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70908-210 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 1.0 g in 50 mL Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.02 g in 50 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:70908-210-02 1 in 1 CARTON 08/01/2018 1 NDC:70908-210-01 50 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/01/2018 Labeler - MeFactory Co., Ltd. (689840967) Registrant - MeFactory Co., Ltd. (689840967) Establishment Name Address ID/FEI Business Operations Cosmax, Inc. 689049693 manufacture(70908-210)