Label: NF SKIN SPF 30 BROAD SPECTRUM MOISTURIZER- titanium dioxide, zinc oxide lotion
- NDC Code(s): 58443-0576-3
- Packager: Prime Enterprises Inc.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated September 20, 2022
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- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warnings
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Directions
- apply liberally 15 minutes before sun exposure
- reapply:
- after 80 minutes of swimming or sweating
- immediately after towel drying
- at least every 2 hours
- 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 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
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INACTIVE INGREDIENT
Allantoin, Alumina, Butyrospermum Parkii (Shea) Butter, Camellia Oleifera (Green Tea) Leaf Extract, Cetyl PEG/PPG-10/1 Dimethicone, Cucumis Sativus (Cucumber) Fruit Extract, Cyclopentasiloxane, Dimethicone Crosspolymer, Disteardimonium Hectorite, Ethylhexylglycerin, Fragrance, Glycerin, Hexyl Laurate, Linum Usitatissimum (Linseed) Seed Oil, Oenothera Biennis (Evening Primrose) Oil, PEG-10 Dimethicone, Phenoxyethanol, Plankton Extract, Polyglyceryl-4 Isostearate, Polymethylsilsesquioxane, Rosa Canina Fruit Oil, Silica, Stearic Acid, Tocopheryl Acetate, Water
- Other Information
- Questions or Comments?
- NF Skin - LuxMD Skin Care SPF 30 Broad Spectrum Moisturizer
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INGREDIENTS AND APPEARANCE
NF SKIN SPF 30 BROAD SPECTRUM MOISTURIZER
titanium dioxide, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58443-0576 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 30.9 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 30.9 mg in 1 mL Inactive Ingredients Ingredient Name Strength POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7) ALLANTOIN (UNII: 344S277G0Z) CUCUMBER (UNII: YY7C30VXJT) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) LINSEED OIL (UNII: 84XB4DV00W) ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ) EVENING PRIMROSE OIL (UNII: 3Q9L08K71N) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STEARIC ACID (UNII: 4ELV7Z65AP) CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60) ALUMINUM OXIDE (UNII: LMI26O6933) SHEA BUTTER (UNII: K49155WL9Y) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) GLYCERIN (UNII: PDC6A3C0OX) HEXYL LAURATE (UNII: 4CG9F9W01Q) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) WATER (UNII: 059QF0KO0R) PHENOXYETHANOL (UNII: HIE492ZZ3T) Product Characteristics Color white (White) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58443-0576-3 50 mL in 1 TUBE; Type 0: Not a Combination Product 06/21/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M020 06/21/2022 Labeler - Prime Enterprises Inc. (101946028) Registrant - Prime Enterprises Inc. (101946028) Establishment Name Address ID/FEI Business Operations Prime Enterprises Inc. 101946028 pack(58443-0576) , manufacture(58443-0576) , label(58443-0576) , analysis(58443-0576)