Label: PHARMACA NATURAL MINERAL SUNSCREEN SPF-50- titanium dioxide, zinc oxide cream
- NDC Code(s): 62082-057-03
- Packager: Pharmaca Integrative Pharmacy, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 5, 2023
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- DRUG FACTS
- Active Ingredients
- Uses:
- Warnings:
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Directions:
Apply liberally 15 minutes before sun exposure. at least every two hours, and immediately after swimming, sweating or towel drying. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use sunscreen with broad-spectrum protection and an SPF rating of 15 or higher. Limit time in sleeve shirts, pants, hats and sunglasses. For children under 6 months, consult a physician. ReapplySun protection measures:Other recommendations:
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Other ingredients:
aqua (deionized water), butyrospermum parkii (shea) butter, camellia sinensis (green tea) extract, cocos nucifera (coconut) oil, eucalyptus globulus (eucalyptus) oil, gluconolactone, glycerin, helianthus annuus (sunflower) seed oil, lecithin, simmondsia chinensis (jojoba) oil, tocopherol (vitamin e), xanthan gum
- For maximum effectiveness:
- Package Labeling:
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INGREDIENTS AND APPEARANCE
PHARMACA NATURAL MINERAL SUNSCREEN SPF-50
titanium dioxide, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62082-057 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 60 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 225 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SHEA BUTTER (UNII: K49155WL9Y) GREEN TEA LEAF (UNII: W2ZU1RY8B0) COCONUT OIL (UNII: Q9L0O73W7L) EUCALYPTUS OIL (UNII: 2R04ONI662) GLUCONOLACTONE (UNII: WQ29KQ9POT) GLYCERIN (UNII: PDC6A3C0OX) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) JOJOBA OIL (UNII: 724GKU717M) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62082-057-03 100 mL in 1 TUBE; Type 0: Not a Combination Product 05/20/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 05/20/2019 Labeler - Pharmaca Integrative Pharmacy, Inc. (031903446)