Label: ANTIBE BEAUSENNE SPECIAL AMPOULE- niacinamide, adenosine gel
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Contains inactivated NDC Code(s)
NDC Code(s): 70929-0002-1, 70929-0002-2 - Packager: Modongee 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 August 22, 2016
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
PURIFIED WATER, BUTYLENE GLYCOL, METHYL GLUCETH-20, HYDROXYETHYL UREA, PEGㆍPPG(18:4) COPOLYMER, BIOSACCHARIDEGUM-1, BETA-GLUCAN, SODIUM HYALURONATE, HYDROLYZED EXTENSIN, HYDROLYZED COLLAGEN, HYDROLYZED ELASTIN, PROPOLIS EXTRACT, PERSIMMON EXTRACT, SODIUM POLYACRYLATE, DIMETHICONE, CYCLOPENTASILOXANE, TRIDECETH-16, PEGㆍPPG(18:18) DIMETHICONE, CAVIAR EXTRACT, RH OLIGOPEPTIDE-1, ALLANTOIN, PANTHENOL, ACRYLATE/C10-30ALKYL ACRYLATE CROSSPOLYMER, CARBOMER, LILIUM CANDIDUM BULB EXTRACT, ALOE VERA EXTRACT, CENTELLA EXTRACT, CHAMOMILE EXTRACT, LICORICE ROOT EXTRACT, GREEN TEA EXTRACT, JAPANESE KNOTWEED EXTRACT, ROSEMARY EXTRACT, GOLD EXTRACT, JAPANESE BEAUTYBERRY EXTRACT, BLUEBERRY EXTRACT, ACAI PALM EXTRACT, POMEGRANATE EXTRACT, FIG EXTRACT, MULBERRY LEAF EXTRACT, GINKGO LEAF EXTRACT, STEARYL ALCOHOL, STEARIC ACID, GLYCERYL STEARATE, HYDROGENATED LECITHIN, COTTON PLANT CELL EXTRACT, HOUTTUYNIA CORDATA EXTRACT, HOP MARJORAM EXTRACT, GREATER GALANGAL LEAF EXTRACT, MULBERRY ROOT EXTRACT, TETRAHEXYL DECYL ASCOBATE, TOCOPHERYL ACETATE, SQUALANE, GLYCERYL LINOLATE/GLYCERYLLINOLATE/GRLYCERYL ARACHIDONATE, SHIITAKE MYCELIUM EXTRACT, CERAMIDE NP, RETINYL PALMITATE, CYCLOPENTASILOXANE, CETYL ETHYL HEXANOATE, PEG-60 HYDROGENATED CASTOR OIL, TRIETHANOLAMINE, ETHYLTEXYL GLYCERIN, PHENOXYETHANOL, DISODIUM EDTA, YELLOW NO.4, YELLOW NO.5, FRAGRANCE
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children - DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ANTIBE BEAUSENNE SPECIAL AMPOULE
niacinamide, adenosine gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70929-0002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 mL NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 2 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) ALLANTOIN (UNII: 344S277G0Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70929-0002-2 4 in 1 BOX 08/22/2016 1 NDC:70929-0002-1 50 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/01/2015 Labeler - Modongee Co., Ltd. (688730710) Registrant - Modongee Co., Ltd. (688730710) Establishment Name Address ID/FEI Business Operations Modongee Co., Ltd. 688730710 manufacture(70929-0002)