Label: DR. MERCOLA SUNSCREEN BROAD SPECTRUM SPF-15- zinc oxide cream
- NDC Code(s): 65121-884-15
- Packager: Pure Source, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 5, 2023
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- DR. MERCOLA Sunscreen Broad Spectrum SPF-15
- Active Ingredient
- Uses
- Warnings
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Directions
- Apply liberally 15 minutes before sun exposure.
- Children under 6 months of age: Ask a doctor.
- 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 value of 15 or higher and other sun protection measures including: Sun Protection Measures:
-
- Limit time in the sun, especially from 10 a.m. - 2 p.m.
- Wear long-sleeve shirts, pants, hats, and sunglasses
- Re-apply:
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- After 40 minutes of swimming or sweating
- Immediately after towel drying
- At least every 2 hours
- Other Information
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Inactive Ingredients
Aqua, Aloe Barbadensis Leaf Juice, Helanthus Annuus (Sunflower) Seed Oil, Lecithin, Cetearyl Alcohol, Cetearyl Glucoside, Cetearyl Olivate, Sorbitan Olivate, Glycerin, Simmonds Chinensia (Jojoba) Seed Oil, Butyrospermum ParkII (Shea) Butter, Camellia Sinensis Leaf Extract, Cocos Nucifera (Coconut) Oil, Glucurolactone, Potassium Sorbate, Xanthan Gum, Punica Granalum Fruit Extract, Tocopherol, Rubus Idaeus (Raspberry) Seed Oil, Astaxanthain Eucalyptus Globulus Leaf Oil.
- DR. MERCOLA Sunscreen Broad Spectrum SPF-15
-
INGREDIENTS AND APPEARANCE
DR. MERCOLA SUNSCREEN BROAD SPECTRUM SPF-15
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65121-884 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 95 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) SUNFLOWER OIL (UNII: 3W1JG795YI) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) CETEARYL OLIVATE (UNII: 58B69Q84JO) SORBITAN OLIVATE (UNII: MDL271E3GR) GLYCERIN (UNII: PDC6A3C0OX) JOJOBA OIL (UNII: 724GKU717M) SHEA BUTTER (UNII: K49155WL9Y) GREEN TEA LEAF (UNII: W2ZU1RY8B0) COCONUT OIL (UNII: Q9L0O73W7L) GLUCUROLACTONE (UNII: XE4Y3016M9) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) XANTHAN GUM (UNII: TTV12P4NEE) POMEGRANATE (UNII: 56687D1Z4D) TOCOPHEROL (UNII: R0ZB2556P8) RASPBERRY SEED OIL (UNII: 9S8867952A) ASTAXANTHIN (UNII: 8XPW32PR7I) EUCALYPTUS OIL (UNII: 2R04ONI662) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65121-884-15 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/09/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 04/28/2014 Labeler - Pure Source, LLC (080354456) Establishment Name Address ID/FEI Business Operations Pure Source, LLC 080354456 manufacture(65121-884)
