Label: ARTISTRY YOUTH XTEND LIFTING SMOOTHING FOUNDATION SHADE BRULE L4W1- octinoxate, oxybenzone cream
- NDC Code(s): 50390-236-00
- Packager: Amway Corp
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 23, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses
- Warnings
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Directions
For suncreen use
- Apply liberally 15 minutes before sun exposure
- Use a water resistant sunscreen if swimming or sweating or washing
- Reapply at least every 2 hours
- Spending time in the sun increases your risk of skin cancer and early skin aging. Sun Protection Measures.
- To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 a.m. – 2 p.m.
- wear long-sleeve shirts, pants, hats, and sunglasses
- Children under 6 months: ask a doctor
- Other Information
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Inactive ingredients
WATER/AQUA/EAU, CYCLOPENTASILOXANE, METHYL TRIMETHICONE, BUTYLENE GLYCOL, GLYCERIN, LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, TALC, DIMETHICONE, TRIMETHYLOLPROPANE TRICAPRYLATE/TRICAPRATE, POLYGLYCERYL-6 POLYRICINOLEATE, HDI/ TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER, DIMETHICONE/PEG-10/15 CROSSPOLYMER, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, PHENOXYETHANOL, SODIUM CHLORIDE, SODIUM CITRATE, POLYGLYCERYL- 3 POLYDIMETHYLSILOXYETHYL DIMETHICONE, TRIETHOXYCAPRYLYLSILANE, ALUMINA, SORBITAN LAURATE, ALUMINUM HYDROXIDE, STEARIC ACID, METHYLPARABEN, SODIUM HYALURONATE, PROPYLPARABEN, FRAGRANCE/ PARFUM, HYDROXYETHYLCELLULOSE, ACETYL DIPEPTIDE-1 CETYL ESTER, ETHYLPARABEN, SILICA, IODOPROPYNYL BUTYLCARBAMATE, LECITHIN, CHLORELLA VULGARIS EXTRACT, GLYCINE SOJA (SOYBEAN) OIL, CERAMIDE-3, LIMNANTHES ALBA (MEADOWFOAM) SEED OIL, BETA-SITOSTEROL, PERILLA OCYMOIDES SEED OIL, SALVIA HISPANICA SEED OIL, OENOTHERA BIENNIS (EVENING PRIMROSE) OIL, TETRAHEXYLDECYL ASCORBATE. MAY CONTAIN/PEUT CONTEINIR: TITANIUM DIOXIDE, IRON OXIDES, BISMUTH OXYCHLORIDE
- Package Labeling:
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INGREDIENTS AND APPEARANCE
ARTISTRY YOUTH XTEND LIFTING SMOOTHING FOUNDATION SHADE BRULE L4W1
octinoxate, oxybenzone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50390-236 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) METHYL TRIMETHICONE (UNII: S73ZQI0GXM) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) GLYCERIN (UNII: PDC6A3C0OX) LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA) TALC (UNII: 7SEV7J4R1U) DIMETHICONE (UNII: 92RU3N3Y1O) TRIMETHYLOLPROPANE TRICAPRYLATE/TRICAPRATE (UNII: N1TRQ06KVJ) POLYGLYCERYL-6 POLYRICINOLEATE (UNII: YPM0ZOC2HR) HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9) DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM CITRATE (UNII: 1Q73Q2JULR) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) ALUMINUM OXIDE (UNII: LMI26O6933) SORBITAN MONOLAURATE (UNII: 6W9PS8B71J) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) STEARIC ACID (UNII: 4ELV7Z65AP) METHYLPARABEN (UNII: A2I8C7HI9T) HYALURONATE SODIUM (UNII: YSE9PPT4TH) PROPYLPARABEN (UNII: Z8IX2SC1OH) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) ACETYL TYROSYLARGININE CETYL ESTER (UNII: 3M7W78X5IR) ETHYLPARABEN (UNII: 14255EXE39) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) CHLORELLA VULGARIS (UNII: RYQ4R60M02) SOYBEAN OIL (UNII: 241ATL177A) CERAMIDE NP (UNII: 4370DF050B) MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y) .BETA.-SITOSTEROL (UNII: S347WMO6M4) PERILLA FRUTESCENS SEED OIL (UNII: 322MS57V7Z) CHIA SEED OIL (UNII: MC2LH51BO7) EVENING PRIMROSE OIL (UNII: 3Q9L08K71N) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50390-236-00 1 in 1 CARTON 05/06/2013 1 30 mL in 1 BOTTLE, PLASTIC; 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 05/06/2013 Labeler - Amway Corp (083416854)
