Label: ARTISTRY SKIN NUTRITION HYDRATING DAY- avobenzone, octisalate, octocrylene lotion
- NDC Code(s): 10056-041-00
- Packager: Access Business Group LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 21, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients (w/w)
- Uses
- Warnings
- Directions
- Other information
-
Inactive ingredients
water, dimethicone, propanediol, butyloctyl salicylate, 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, dipropylene glycol, disodium EDTA, isononyl isononanoate, , tocopherol, glycine soja (soybean) oil, maltodextrin, citric acid, lecithin, centipeda cunninghamii extract, pentadecalactone, salvia hispanica seed extract, carrageenan, punica granatum fruit extract, zinc PCA, rubus fruticosus (blackberry) leaf extract, ceramide NP, sea salt, beta-sitosterol, sodium hyaluronate, oenothera biennis (evening primrose) oil, perilla ocymoides seed oil, helianthus annuus (sunflower) seed oil, BHT
- Questions?
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
ARTISTRY SKIN NUTRITION HYDRATING DAY
avobenzone, octisalate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10056-041 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 70 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) PROPANEDIOL (UNII: 5965N8W85T) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) 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) DIPROPYLENE GLYCOL (UNII: E107L85C40) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) TOCOPHEROL (UNII: R0ZB2556P8) SOYBEAN OIL (UNII: 241ATL177A) MALTODEXTRIN (UNII: 7CVR7L4A2D) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PENTADECALACTONE (UNII: OK17S3S98K) CARRAGEENAN (UNII: 5C69YCD2YJ) POMEGRANATE (UNII: 56687D1Z4D) ZINC PIDOLATE (UNII: C32PQ86DH4) RUBUS FRUTICOSUS LEAF (UNII: YQ2S06L8S9) 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:10056-041-00 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)