Label: BASS PRO SHOPS MINERAL SUN STICK SUNSCREEN BROAD SPEC SPF 40- titanium dioxide, zinc oxide cream
- NDC Code(s): 14268-125-01
- Packager: ENGLEWOOD LAB, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Uses
- Warnings
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Directions
• Apply liberally 15 minutes before sun exposure • • after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours • Children under 6 months: Ask a doctor • Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the 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 10a.m. - 2p.m. • Wear long-sleeved shirts, pants, hats and sunglasses
Reapply:Sun Protection Measures: - Other Information
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Inactive Ingredients
Polyethylene, Dimethicone, Butyloctyl Salicylate, Petrolatum, Butyrospermum Parkii (Shea) Butter, C12-15 Alkyl Benzoate, Caprylic/Capric Triglyceride, Methyl Dihydroabietate, Acrylates/ Ethylhexyl Acrylate/Dimethicone Methacrylate Copolymer, Octyldodecanol, Tetrahexyldecyl Ascorbate (Vitamin C), Tocopherol (Vitamin E), Behenyl Olivate, Aluminum Hydroxide, Stearic Acid, Sorbitan Sesquioleate, Glyceryl Isostearate, Polyhydroxystearic Acid, Citric Acid, Benzylidene Dimethoxydimethylindanone.
- Package Labeling:
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INGREDIENTS AND APPEARANCE
BASS PRO SHOPS MINERAL SUN STICK SUNSCREEN BROAD SPEC SPF 40
titanium dioxide, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:14268-125 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 81 mg in 1 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 60 mg in 1 g Inactive Ingredients Ingredient Name Strength HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) DIMETHICONE (UNII: 92RU3N3Y1O) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) PETROLATUM (UNII: 4T6H12BN9U) SHEA BUTTER (UNII: K49155WL9Y) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F) OCTYLDODECANOL (UNII: 461N1O614Y) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) TOCOPHEROL (UNII: R0ZB2556P8) BEHENYL OLIVATE (UNII: NGS1GGK4GW) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) STEARIC ACID (UNII: 4ELV7Z65AP) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) BENZYLIDENE DIMETHOXYDIMETHYLINDANONE (UNII: 75HIF3C97L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:14268-125-01 17 g in 1 TUBE; Type 0: Not a Combination Product 04/19/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 04/19/2023 Labeler - ENGLEWOOD LAB, INC. (172198223) Establishment Name Address ID/FEI Business Operations ENGLEWOOD LAB, INC. 172198223 manufacture(14268-125) , label(14268-125)
