Label: BARE REPUBLIC BIG ADVENTURE STICK SPF 70- titanium dioxide 3.5% zinc oxide 16.9% stick
- NDC Code(s): 79753-026-01
- Packager: COOLA
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 20, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
Directions
Apply liberally 15 minutes before sun exposure
• reapply: • after 80 minutes 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 a broad spectrum SPF of 15
or higher and after 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 INGREDIENT
Inactive Ingredients
Helianthus Annuus (Sunflower) Seed Wax,
Neopentyl Glycol Diheptanoate, C12-15 Alkyl
Benzoate, Isododecane, Behenyl Behenate,
Caprylic/Capric Triglyceride, Lauryl Laurate,
Polyhydroxystearic Acid, Butyrospermum Parkii
(Shea) Butter, Ethylhexyl Methoxycrylene, Methyl
Dihydroabietate, Stearyl/Octyldodecyl Citrate
Crosspolymer, Polymethylsilsesquioxane,
Trimethoxybenzylidene Pentanedione, Triethyl
Citrate, Ethyl Ferulate, Triethoxycaprylylsilane,
1,2-Hexanediol, Caprylyl Glycol, Euphorbia Cerifera
(Candelilla) Wax, Stearic Acid, Alumina,
Gamma-Decalactone, Raspberry Ketone, Isostearic
Acid, Vanillin, Gamma-Nonalactone, Gamma
Octalactone, Lecithin, Polyglyceryl-3 Polyricinoleate,
Allyl Heptoate, Heliotropine, Vitis Vinifera (Grape)
Seed Extract, Daucus Carota Sativa (Carrot) Root
Extract, Rubus Idaeus (Raspberry) Fruit Extract. - OTHER SAFETY INFORMATION
- QUESTIONS
- Package for BARE REPUBLIC MINERAL Sunscreen Stick
-
INGREDIENTS AND APPEARANCE
BARE REPUBLIC BIG ADVENTURE STICK SPF 70
titanium dioxide 3.5% zinc oxide 16.9% stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79753-026 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 3.5 g in 100 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 16.9 g in 100 g Inactive Ingredients Ingredient Name Strength HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV) NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) ISODODECANE (UNII: A8289P68Y2) BEHENYL BEHENATE (UNII: K8NU647RJ0) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) LAURYL LAURATE (UNII: GPW77G0937) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) SHEA BUTTER (UNII: K49155WL9Y) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F) STEARYL/OCTYLDODECYL CITRATE CROSSPOLYMER (UNII: PN88NW0KPK) POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK) TRIMETHOXYBENZYLIDENE PENTANEDIONE (UNII: 322V0ACF25) TRIETHYL CITRATE (UNII: 8Z96QXD6UM) ETHYL FERULATE (UNII: 5B8915UELW) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CANDELILLA WAX (UNII: WL0328HX19) STEARIC ACID (UNII: 4ELV7Z65AP) ALUMINUM OXIDE (UNII: LMI26O6933) .GAMMA.-DECALACTONE (UNII: 7HLS05KP9O) 4-(P-HYDROXYPHENYL)-2-BUTANONE (UNII: 7QY1MH15BG) ISOSTEARIC ACID (UNII: X33R8U0062) VANILLIN (UNII: CHI530446X) .GAMMA.-NONALACTONE (UNII: I1XGH66S8P) .GAMMA.-OCTALACTONE (UNII: UHD6M52X0K) LECITHIN, SUNFLOWER (UNII: 834K0WOS5G) POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4) ALLYL HEPTANOATE (UNII: AU4CYG9V68) PIPERONAL (UNII: KE109YAK00) VITIS VINIFERA SEED (UNII: C34U15ICXA) CARROT (UNII: L56Z1JK48B) RASPBERRY (UNII: 4N14V5R27W) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79753-026-01 56 g in 1 TUBE; Type 0: Not a Combination Product 02/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/01/2022 Labeler - COOLA (956990290) Registrant - Bentley Laboratories, LLC (068351753) Establishment Name Address ID/FEI Business Operations Bentley Laboratories, LLC 068351753 manufacture(79753-026)