Label: BARE REPUBLIC MINERAL SHIMMER SPF 30 GOLDEN DAZE- titanium dioxide, zinc oxide lotion
- NDC Code(s): 79753-066-01
- Packager: COOLA, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated May 22, 2024
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- ACTIVE INGREDIENT
- PURPOSE
- Uses
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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Directions
- Shake well. Apply liberally 15 minutes before sun exposure
- Reapply: • After 40 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 a 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
- OTHER SAFETY INFORMATION
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INACTIVE INGREDIENT
Aloe Barbadensis Leaf Juice, Aluminum Hydroxide, Amethyst Powder, Bisabolol, Butyloctyl Salicylate, Calcium Sodium Borosilicate, Caprylhydroxamic Acid, Caprylyl Glycol, Cetearyl Alcohol, Cetyl Alcohol, Citric Acid, Coco-Glucoside, Cocos Nucifera (Coconut) Oil, Fragrance, Glycerin, Glyceryl Stearate, Helianthus Annuus (Sunflower) Seed Oil, Iron Oxides, Mica, Moringa Oleifera Seed Oil, Polyhydroxystearic Acid, Silica, Sodium Gluconate, Sodium Stearoyl Glutamate, Stearic Acid, Tocopherol, Water, Xanthan Gum
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INGREDIENTS AND APPEARANCE
BARE REPUBLIC MINERAL SHIMMER SPF 30 GOLDEN DAZE
titanium dioxide, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79753-066 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 6.4 g in 100 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 4.2 g in 100 mL Inactive Ingredients Ingredient Name Strength COCONUT OIL (UNII: Q9L0O73W7L) ALOE VERA LEAF (UNII: ZY81Z83H0X) SODIUM GLUCONATE (UNII: R6Q3791S76) CAPRYLYL GLYCOL (UNII: 00YIU5438U) GLYCERIN (UNII: PDC6A3C0OX) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) TOCOPHEROL (UNII: R0ZB2556P8) XANTHAN GUM (UNII: TTV12P4NEE) STEARIC ACID (UNII: 4ELV7Z65AP) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CALCIUM ALUMINUM BOROSILICATE (UNII: 3JRB8A35M0) MICA (UNII: V8A1AW0880) WATER (UNII: 059QF0KO0R) FERRIC OXIDE RED (UNII: 1K09F3G675) MORINGA OLEIFERA SEED OIL (UNII: REM6A5QMC0) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETYL ALCOHOL (UNII: 936JST6JCN) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) LEVOMENOL (UNII: 24WE03BX2T) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M) COCO GLUCOSIDE (UNII: ICS790225B) SUNFLOWER OIL (UNII: 3W1JG795YI) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79753-066-01 100 mL in 1 TUBE; Type 0: Not a Combination Product 12/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 12/01/2018 Labeler - COOLA, LLC (956990290)