- Active ingredient(s)
- Purpose
- Uses
- Warnings
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Directions
- apply liberally 15 minutes before sun exposure
- reapply at least every 2 hours
- use a water resistant sunscreen if swimming or sweating.
- Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. 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 of age: Ask a doctor
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Inactive Ingredients
Purified Water, Cyclopentasiloxane, Isononyl lsononanoate, Phenyl Trimethicone, Alcohol Denat., Lauryl PEG-8 Dimethieone, Disteardimonium Hectorite, Sodium Chloride, PEG-10 Dimethicone, Talc, Caprylyl Glycol, ALumina, Stearic Acid, Phenoxyethanol, Potassium Sorbate, Sodium Dehydroacetate, Methicone, Hexylene Glycol, Propanediol, Tocopheryl Acetate, Hydrogen Dimethicone, Boerhavia Diffusa Root Extract, Ascorbyl Palmitate.
MAY CONTAIN: Iron Oxides (CI 77491, CI 77492, CI77499), Titanium Dioxide (CI77891). - Other information
- QUESTIONS OR COMMENTS?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ULTA BEAUTY TINTED MOISTURIZER SPF-30
octinoxate, titanium dioxide, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62296-0118 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 g in 100 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 3.5 g in 100 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 3 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R) ALCOHOL (UNII: 3K9958V90M) PEG-8 DIMETHICONE (UNII: GIA7T764OD) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ALUMINUM OXIDE (UNII: LMI26O6933) STEARIC ACID (UNII: 4ELV7Z65AP) PHENOXYETHANOL (UNII: HIE492ZZ3T) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) METHICONE (20 CST) (UNII: 6777U11MKT) HEXYLENE GLYCOL (UNII: KEH0A3F75J) PROPANEDIOL (UNII: 5965N8W85T) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI) BOERHAVIA DIFFUSA ROOT (UNII: KR0SR09KYL) ASCORBYL PALMITATE (UNII: QN83US2B0N) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62296-0118-1 35 mL in 1 TUBE; Type 0: Not a Combination Product 09/27/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 08/17/2015 Labeler - Ulta (608168597)