Label: LUMINESS SPF30 SUNCREEN SETTING POWDER- zinc oxide,titanium dioxide powder
- NDC Code(s): 73368-150-18
- Packager: Kinetics Derma Beauty, L.L.C
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 12, 2024
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- Inactive Ingredients
- Luminess SPF 30 Active Ingredients
- Luminess SPF 30 dosage and administration
- Luminess SPF 30 Keep out of reach of children
- Luminess SPF 30 Purpose
- Luminess SPF 30 Usage
- Luminess SPF 30 warnings
- Luminess SPF Instructions for use
- Luminess SPF 30 Principle display panel
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INGREDIENTS AND APPEARANCE
LUMINESS SPF30 SUNCREEN SETTING POWDER
zinc oxide,titanium dioxide powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73368-150 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.0375 g in 0.15 g TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.012 g in 0.15 g Inactive Ingredients Ingredient Name Strength POTASSIUM HYDROLYZED JOJOBA ESTERS (UNII: CH428W5O62) BISMUTH OXYCHLORIDE (UNII: 4ZR792I587) CHLORPHENESIN (UNII: I670DAL4SZ) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) MAGNESIUM MYRISTATE (UNII: Z1917F0578) MICA (UNII: V8A1AW0880) THEOBROMA GRANDIFLORUM SEED BUTTER (UNII: I711F13FXM) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) BORON NITRIDE (UNII: 2U4T60A6YD) ISOPROPYL ALCOHOL (UNII: ND2M416302) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73368-150-18 18 g in 1 CARTON; Type 0: Not a Combination Product 08/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 08/01/2020 04/01/2026 Labeler - Kinetics Derma Beauty, L.L.C (117146776) Registrant - Kinetics Derma Beauty, L.L.C (117146776) Establishment Name Address ID/FEI Business Operations Kinetics Derma Beauty, L.L.C 117146776 manufacture(73368-150)