Label: ALEX MD PHD SHEER MINERAL SUNSCREEN- zinc oxide, titanium dioxide cream
- NDC Code(s): 78709-001-01
- Packager: PHYSICIAN LABORATORIES INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 28, 2025
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- KEEP OUT OF REACH OF CHILDREN
-
Directions
- Apply liberally 15 minutes before sun exposure.
- Reapply:
- After 80 minutes of swimmingor sweating.
- Immediately after towel drying.
- At least every 2 hours.
- Children under 6 months: Ask a doctor.
- 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 10am–2pm.
•Wear long-sleeved shirts, pants, hats, and sunglasses. -
Inactive igredients
Cyclopentasiloxane, Water/Aqua/Eau, Coco-Caprylate/Caprate, Isononyl Isononanoate, Polyglyceryl-3 Polydimethylsiloxyethyl
Dimethicone, HDI/Trimethylol Hexyllactone Crosspolymer, Methyl Methacrylate Crosspolymer, Glycerin,Aluminum Hydroxide, Stearic Acid,
Disteardimonium Hectorite, Undaria Pinnatifida Extract, Triethoxysilylethyl Polydimethylsiloxyethyl Hexyl Dimethicone,Astrocaryum Tucuma Seed
Butter, Butyrospermum Parkii (Shea) Butter, Theobroma Grandiflorum Seed Butter, Tetrahexyldecyl Ascorbate,Dunaliella Salina Extract, Bisabolol, Ubiquinone,Ergothioneine, Tremella Fuciformis Sporocarp Extract, Tocopheryl Acetate,Betaine, Polyglyceryl-3 Diisostearate,Caprylyl Glycol, Caprylhydroxamic Acid, Squalane, Polyglyceryl-3 Polyricinoleate,C12-15 Alkyl Benzoate, Disodium EDTA, Sodium Chloride, Phenoxyethanol,
Ethylhexylglycerin, Potassium Sorbate, Sodium Benzoate, Lavandula Angustifolia (Lavender) Oil, Citrus Aurantium Dulcis (Orange) Peel Oil - Other information
- Product label
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INGREDIENTS AND APPEARANCE
ALEX MD PHD SHEER MINERAL SUNSCREEN
zinc oxide, titanium dioxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:78709-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 20.2 g in 100 g TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (CI 77891 - UNII:15FIX9V2JP) TITANIUM DIOXIDE 6.8 g in 100 g Inactive Ingredients Ingredient Name Strength CYCLOPENTASILOXANE (UNII: 0THT5PCI0R) WATER (UNII: 059QF0KO0R) COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q) METHYL METHACRYLATE (UNII: 196OC77688) GLYCERIN (UNII: PDC6A3C0OX) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) STEARIC ACID (UNII: 4ELV7Z65AP) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) UNDARIA PINNATIFIDA (UNII: ICV1OK7M1S) TRIETHOXYSILYLETHYL POLYDIMETHYLSILOXYETHYL HEXYL DIMETHICONE (UNII: X75PL53TZJ) ASTROCARYUM VULGARE KERNEL OIL (UNII: 1IQY04O559) SHEA BUTTER (UNII: K49155WL9Y) THEOBROMA GRANDIFLORUM SEED BUTTER (UNII: I711F13FXM) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) DUNALIELLA SALINA (UNII: F4O1DKI9A6) LEVOMENOL (UNII: 24WE03BX2T) UBIDECARENONE (UNII: EJ27X76M46) ERGOTHIONEINE (UNII: BDZ3DQM98W) TREMELLA FUCIFORMIS FRUITING BODY (UNII: GG8N28393G) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) BETAINE (UNII: 3SCV180C9W) POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) SQUALANE (UNII: GW89575KF9) POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) EDETATE DISODIUM (UNII: 7FLD91C86K) SODIUM CHLORIDE (UNII: 451W47IQ8X) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) LAVENDER OIL (UNII: ZBP1YXW0H8) ORANGE OIL, COLD PRESSED (UNII: AKN3KSD11B) HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:78709-001-01 1 in 1 CARTON 03/19/2025 1 65 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 03/19/2025 Labeler - PHYSICIAN LABORATORIES INC (078503839)
