Label: WARRIOR BROAD SPECTRUM SPF 30 SUNSCREEN MINERALS FORMULA- titanium dioxide, zinc oxide lotion
- NDC Code(s): 58443-0645-3
- Packager: Prime Enterprises Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 10, 2024
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- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warnings
-
Directions
- apply liberally 15 minutes before sun exposure
- reapply
- after 80 minutes of swimming or sweating
- immediately after towel drying
- at least every two 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
-
Inactive Ingredients
Acrylic Acid/VP Crosspolymer, Allantoin, Aluminum Hydroxide, Butoctyl Salicylate, C12-15 Alkyl Benzoate, C13-15 Alkane, Camellia Oleifera (Green Tea) Leaf Extract, Capryl Glycol, Ceteareth-20, Cetyl Alcohol, Decyl Glucoside, Ethyl Ferulate, Glycerin, Isododecane, Isohexadecane, Phenoxyethanol, Polyglyceryl-3 Distearate, Sodium Hydroxide, Stearic Acid, Stearyl Alcohol, Triethoxycaprylylsilane, VP/Acrylates/Lauryl Methacrylate Copolymer, Water
- Other Information
- Warrior 30 Broad Spectrum SPF 30 Sunscreen Minerals Formula
-
INGREDIENTS AND APPEARANCE
WARRIOR BROAD SPECTRUM SPF 30 SUNSCREEN MINERALS FORMULA
titanium dioxide, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58443-0645 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 29.7 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 29.7 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) C13-15 ALKANE (UNII: 114P5I43UJ) CAPRYLYL GLYCOL (UNII: 00YIU5438U) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) CETYL ALCOHOL (UNII: 936JST6JCN) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) ETHYL FERULATE (UNII: 5B8915UELW) STEARIC ACID (UNII: 4ELV7Z65AP) ISODODECANE (UNII: A8289P68Y2) ISOHEXADECANE (UNII: 918X1OUF1E) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60) POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV) SODIUM HYDROXIDE (UNII: 55X04QC32I) PHENOXYETHANOL (UNII: HIE492ZZ3T) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) TRIETHOXYSILANE (UNII: 8T460WDH89) ALLANTOIN (UNII: 344S277G0Z) Product Characteristics Color white (Off White) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58443-0645-3 88.7 mL in 1 TUBE; Type 0: Not a Combination Product 10/31/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 10/31/2023 Labeler - Prime Enterprises Inc. (101946028) Registrant - Prime Enterprises Inc. (101946028) Establishment Name Address ID/FEI Business Operations Prime Enterprises Inc. 101946028 pack(58443-0645) , manufacture(58443-0645) , label(58443-0645) , analysis(58443-0645)