ALEX MD PHD SHEER MINERAL SUNSCREEN- zinc oxide, titanium dioxide cream

ALEX MD PHD Sheer Mineral Sunscreen by

Drug Labeling and Warnings

ALEX MD PHD Sheer Mineral Sunscreen by is a Otc medication manufactured, distributed, or labeled by PHYSICIAN LABORATORIES INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Zinc Oxide, 20.2%
Titanium Dioxide, 6.8%

Purpose

Sunscreen

Uses

• Helps prevent sunburn
• If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early

Warnings

• For external use only
• Do not use ondamaged or broken skin.
• When using this productkeep out of eyes. Rinse with water to remove.
• Stop use and ask a doctorif rash occurs.
• Keep out of reach of children.If product is swallowed, get medical help or contact a Poison Control Center right away.

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

Protect this product from excessive heat and direct sun.

Product label

INGREDIENTS AND APPEARANCE

ALEX MD PHD SHEER MINERAL SUNSCREEN 
zinc oxide, titanium dioxide cream

Product 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)