Label: THE FACT NATURAL SPN18 - THE JUNIORCREAM- niacinamide, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 77049-0002-1 - Packager: Interkos Co.,Ltd.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated May 3, 2020
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
water, butylene glycol, glycerin, dimethicone, cyclopentasiloxane, illicium verum(anise) fruit extract, allantoin, synthetic fluorphlogopite, disodium edta, tocopheryl acetate, alcohol, caffeine, titanuim dioxide, sodium hyaluronate, brassica oleracea italica (broccoli) extract, scutellaria baicalensis root extract, mica, bht, glycyrrhiza glabra (licorice) root extract, polygonum multiflorum root extract, phellinus linteus extract, morus alba bark extract, sophora flavescens root extract, sesamum indicum ( sesame) seed extract, angelica gigas root extract, sigesbeckia orientalis extract, paeonia lactiflora extract, cimicifuga racemosa root extract, peg-40 hydrogenated castor oil, dipeptide diaminobutyroyl benzylamide diacetate, ppg-26-buteth-26, triethoxycaprylylsilane, camellia sinensis leaf extract, ethylhexylglycerin, prunus serrulata flower extract, nymphaea alba flower extract, nelumbium speciosum flower extract, camellia japonica flower extract, rosa hybrid flower extract, palmitoyl tripeptide-1, tripeptide-1, copper tripeptide-1, acetyl hexapeptide-8, palmitoyl pentapeptide-4, hexapeptide-9, nonapeptide-1, oleth-5, bis-peg18 methyl ether dimethyl silane, silica, ammonium acryloyldimethyltaurate/vp copolymer, hydrogenated lecithin, sorbitol, trehalose, caprylyl glycol, dimethicone/vinyl dimethicone crosspolymer, carbomer, tromethamine, 1,2-hexanediol
- 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 JUNIORCREAM
niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77049-0002 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:77049-0002-1 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(77049-0002)
