Label: THE FACT NATURAL SPN18 - THE SENIORCREAM- niacinamide, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 77049-0001-1 - Packager: Interkos Co.,Ltd.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated May 2, 2020
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
water, butylene glycol, glycerin, dimethicone, cyclopentasiloxane, illicium verum(anise) fruit extract, allantoin, synthetic fluorphlogopite, tocopheryl acetate, disodium edta, acacia senegal gum, alcohol, cafeine, titanium dioxide, sodium hyaluronate, brassica oleracea italica (broccoli) extract, peat water, hydroxypropyl methylcellulose, citric acid, scutellaria baicalensis root extract, mica, BHT, sesamum indicum(sesame) seed extract, sophora flavescens root extract, phellinus linteus extract, sigesbeckia orientalis extract, cimicifuga racemosa root extract, paeonia lactiflora extract, polygonum multiflorum root extract, morus alba bark extract, glycyrrhiza glabra(licorice) root extract, angelica gigas root extract, PEG-40 hydrogenated castor oil, potassium sorbate, dipeptide diaminobutryroyl benzylamide diacetate, PPG-26-Buteth-26, triethoxycaprylylsilane, camellia sinensis leaf extract, ethylhexylglycerin, nelumbium speciosum flower extract, prunus serrulata flower extract, nymphaea alba flower extract, camellia japonica flower extract, rosa hybrid flower extract, palmitoyl pntapeptide-4, acetyl hexapeptide-8, tripeptide-1, palmitoyl tripeptide-1, copper tripeptide-1, hexapeptide-9, nonapeptide-1, oleth-5, ammonium acryloyldimethytaurate/vp copolymer, silica, BIS-PEG-18 methyl ether dimethyl silane, hydrogenated lecithin, sorbitol, trehalose, caprylrl glycol, dimethicone/vinyl dimethicone crosspolymer, carbomer, tromethamine, 1,2-hexanediol, fragrance
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
THE FACT NATURAL SPN18 - THE SENIORCREAM
niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77049-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 3 g in 100 mL ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 mL Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL (UNII: 3XUS85K0RA) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77049-0001-1 30 mL in 1 CONTAINER; Type 0: Not a Combination Product 05/02/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/02/2020 Labeler - Interkos Co.,Ltd. (689850314) Registrant - Interkos Co.,Ltd. (689850314) Establishment Name Address ID/FEI Business Operations Interkos Co.,Ltd. 689850314 manufacture(77049-0001)