Label: ARTISTRY SKIN NUTRITION BALANCING MATTE DAY- avobenzone, octisalate, octocrylene lotion
- NDC Code(s): 10056-040-00
- Packager: Access Business Group LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 21, 2023
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Inactive ingredients
water, dimethicone, butyloctyl salicylate, propanediol, cetearyl alcohol, glycerin, polysorbate 80, butylene glycol, ammonium acryloyldimethyltaurate/ VP copolymer, phenoxyethanol, salvia hispanica seed oil, calcium sodium borosilicate, cetearyl glucoside, tocopheryl acetate, chlorphenesin, malpighia emarginata (acerola) fruit extract, pentylene glycol, allantoin, carnosine, dipotassium glycyrrhizate, fragrance/parfum, kaolin, disodium EDTA, isononyl isononanoate, dipropylene glycol, tocopherol, glycine soja (soybean) oil, maltodextrin, citric acid, lecithin, centipeda cunninghamii extract, salvia hispanica seed extract, carrageenan, pentadecalactone, punica granatum fruit extract, zinc PCA, rubus fruticosus (blackberry) leaf extract, spiraea ulmaria extract, ceramide NP, sea salt, beta-sitosterol, sodium hyaluronate, oenothera biennis (evening primrose) oil, perilla ocymoides seed oil, helianthus annuus (sunflower) seed oil, BHT
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INGREDIENTS AND APPEARANCE
ARTISTRY SKIN NUTRITION BALANCING MATTE DAY
avobenzone, octisalate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10056-040 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 40 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) PROPANEDIOL (UNII: 5965N8W85T) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) GLYCERIN (UNII: PDC6A3C0OX) POLYSORBATE 80 (UNII: 6OZP39ZG8H) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG) PHENOXYETHANOL (UNII: HIE492ZZ3T) CHIA SEED OIL (UNII: MC2LH51BO7) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CHLORPHENESIN (UNII: I670DAL4SZ) ACEROLA (UNII: XDD2WEC9L5) PENTYLENE GLYCOL (UNII: 50C1307PZG) ALLANTOIN (UNII: 344S277G0Z) CARNOSINE (UNII: 8HO6PVN24W) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) KAOLIN (UNII: 24H4NWX5CO) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) DIPROPYLENE GLYCOL (UNII: E107L85C40) TOCOPHEROL (UNII: R0ZB2556P8) SOYBEAN OIL (UNII: 241ATL177A) MALTODEXTRIN (UNII: 7CVR7L4A2D) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CHIA SEED (UNII: NU0OLX06F8) CARRAGEENAN (UNII: 5C69YCD2YJ) PENTADECALACTONE (UNII: OK17S3S98K) POMEGRANATE (UNII: 56687D1Z4D) ZINC PIDOLATE (UNII: C32PQ86DH4) RUBUS FRUTICOSUS LEAF (UNII: YQ2S06L8S9) FILIPENDULA ULMARIA ROOT (UNII: 997724QNDS) CERAMIDE NP (UNII: 4370DF050B) SEA SALT (UNII: 87GE52P74G) .BETA.-SITOSTEROL (UNII: S347WMO6M4) HYALURONATE SODIUM (UNII: YSE9PPT4TH) EVENING PRIMROSE OIL (UNII: 3Q9L08K71N) PERILLA FRUTESCENS SEED OIL (UNII: 322MS57V7Z) SUNFLOWER OIL (UNII: 3W1JG795YI) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10056-040-00 1 in 1 CARTON 04/04/2021 1 50 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 04/04/2021 Labeler - Access Business Group LLC (839830713)