- ACTIVE INGREDIENT
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INSTRUCTIONS FOR USE
Apply in the morning, as the last product in your regiment or as needed, at least every 2 hours if in direct sunlight. 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 Broad Spectrum SPF Value of 15 or higher and other sun protection measures including limiting time in the sun, especially from 10 a.m. to 2 p.m., wear long sleeved shirts, pants, hats and sunglasses, children under 6 months of age: ask a doctor.
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DOSAGE & ADMINISTRATION
Apply in the morning, as the last product in your regiment or as needed, at least every 2 hours if in direct sunlight. 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 Broad Spectrum SPF Value of 15 or higher and other sun protection measures including limiting time in the sun, especially from 10 a.m. to 2 p.m., wear long sleeved shirts, pants, hats and sunglasses, children under 6 months of age: ask a doctor.
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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INACTIVE INGREDIENT
Water, Butyloctyl Salicylate, Fatty Alcohol, Ethoxylated Sorbitan Ester, Sodium Hyaluronate, TRIETHOXYCAPRYLYLSILANE, Polysorbate 60, Heptyl Undecylenate, 4-t-Butylcyclohexanol, Dimethicone, Ethylhexyl Methoxycrylene, Caesalpinia Spinosa Fruit Pod Extract, Helianthus Annuus (Sunflower) Sprout Extract, Sodium Benzoate, BENZYL ALCOHOL, BENZOIC ACID, SORBIC ACID, CAPRYLIC/CAPRIC TRIGLYCERIDE, pOLYHYDROXYSTEARIC ACID, ALUMINA, STEARIC ACID, Butylene Glycol, Pentylene Glycol, Hydroxyphenyl Propamidobenzoic Acid, Ubiquinone, Tocopheryl Acetate, C12-15 Alkyl Benzoate, Phenoxyethanol, Disodium EDTA, NIACINAMIDE, Bisabolol, Hydroxymethoxyphenyl Decanone, Butylated hydroxytoluene, sODIUM ascorbyl phosphate, linalool, iron oxides
- INDICATIONS & USAGE
- PURPOSE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RADIANCESHIELD GOLDEN TINT
radianceshield golden tint lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71393-017 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 10.5 g in 100 g TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 4.4 g in 100 g Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP) 2,3-DICHLOROBENZOIC ACID (UNII: CGP39QV5WF) POLYSORBATE 60 (UNII: CAL22UVI4M) BENZYL ALCOHOL (UNII: LKG8494WBH) MAGNESIUM DISODIUM EDTA (UNII: NDT563S5VZ) 4-HYDROXYBENZYL ALCOHOL (UNII: 1A3AH1FP1B) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) HEPTYL UNDECYLENATE (UNII: W77QUB6GXO) WATER (UNII: 059QF0KO0R) OMEGA-3 FATTY ACIDS (UNII: 71M78END5S) .ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC) UBIDECARENONE (UNII: EJ27X76M46) PENTYLENE GLYCOL (UNII: 50C1307PZG) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) HELIANTHUS ANNUUS WHOLE (UNII: 17S27ZT6KR) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM BENZOATE (UNII: OJ245FE5EU) SORBIC ACID (UNII: X045WJ989B) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) 1-(4-HYDROXY-3-METHOXYPHENYL)-DECAN-3-ONE (UNII: BO24ID7E9U) BROWN IRON OXIDE (UNII: 1N032N7MFO) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) ALUMINUM OXIDE (UNII: LMI26O6933) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CAESALPINIA SPINOSA WHOLE (UNII: O759MFY23D) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) 4-TERT-BUTYLCYCLOHEXANOL, CIS- (UNII: L5067JRJ73) SORBITAN MONOOLEATE (UNII: 06XEA2VD56) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR) HYALURONATE SODIUM (UNII: YSE9PPT4TH) DIMETHICONE 200 (UNII: RGS4T2AS00) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) LINALOOL, (+/-)- (UNII: D81QY6I88E) NIACINAMIDE (UNII: 25X51I8RD4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71393-017-34 115 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/31/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/31/2018 Labeler - The Skin Atelier, Inc. (135049810) Establishment Name Address ID/FEI Business Operations The Skin Atelier, Inc 135049810 manufacture(71393-017)