CVS SPF 50 FACE SUNSCREEN- titanium dioxide, zinc oxide lotion

CVS SPF 50 Face Sunscreen by

Drug Labeling and Warnings

CVS SPF 50 Face Sunscreen by is a Otc medication manufactured, distributed, or labeled by CVS, Derma Care Research Labs, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Titanium Dioxide 6%, Zinc Oxide 5%

PURPOSE

Sunscreen

INDICATIONS & USAGE

Helps prevent sunscreen. If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

WARNINGS

For external use only.

Do not use on damaged or broken skin.

When using this product avoid contact with eyes. Rinse with water to remove.

Stop use and ask a doctor if rash or irritation develops and lasts.

KEEP OUT OF REACH OF CHILDREN

If product is swallowed, get medical help or contact a poison Control Center right away.

DOSAGE & ADMINISTRATION

For sunscreen use: shake well before use, apply liberally 15 minutes before sun exposure and as needed, reapply: after 40 minutes of swimming or sweating, immediately after towel drying, and 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 value of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 am - 2 pm, wear long-sleeved shirts, pants, hats, and sunglasses.

Children under 6 months of age: ask a doctor.

INACTIVE INGREDIENT

Aloe barbadensis leaf extract, alumina, aluminum starch octenylsuccinate, benzyl alcohol, C12-15 alkyl benzoate, camellia sinensis leaf extract, cetyl PEG/PPG-10/1 dimethicone, cucumis sativus (cucumber) fruit extract, dimethicone, disodium EDTA, ethyhexyl palmitate, ethyhexylglycerin, glycerin, hydrogen dimethicone, propanediol, punica granatum fruit juice, silica, sodium chloride, sorbitan olivate, styrene/acrylates copolymer, vitis vinifera (grape) seed extract, water.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CVS SPF 50 FACE SUNSCREEN 
titanium dioxide, zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51316-217
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	5 g  in 100 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	6 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN DIMETHICONE (40 CST) (UNII: T8RBB3RCP9)
PROPANEDIOL (UNII: 5965N8W85T)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
WATER (UNII: 059QF0KO0R)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
ALUMINA (UNII: LMI26O6933)
CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0)
CUCUMBER (UNII: YY7C30VXJT)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
PUNICA GRANATUM FRUIT JUICE (UNII: 99S671U9KB)
SORBITAN OLIVATE (UNII: MDL271E3GR)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
VITIS VINIFERA (GRAPE) SEED (UNII: C34U15ICXA)
DIMETHICONE 200 (UNII: RGS4T2AS00)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51316-217-01	1 in 1 BOX	01/28/2025
1		50 mL in 1 BOTTLE; 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	01/28/2025

Labeler - CVS (062312574)

Registrant - Derma Care Research Labs, LLC (116817470)

Establishment
Name	Address	ID/FEI	Business Operations
Derma Care Research Labs, LLC		116817470	manufacture(51316-217)