CVS SPF 50 Face Sunscreen

Manufacturer
CVS | Derma Care Research Labs, LLC
Effective date
2025-09-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:14:08

Label at a glance#

ProductCVS SPF 50 Face Sunscreen
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 6%, Zinc Oxide 5%

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

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 SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

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 SECTION

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

cartoncarton

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51316-217-01CVS SPF 50 Face Sunscreen50 mL in 1 BOTTLELOTION502
51316-217-01CVS SPF 50 Face Sunscreen1 in 1 BOXLOTION12

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51316-21751316-217-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CVS SPF 50 Face SunscreenTITANIUM DIOXIDE, ZINC OXIDECVS26a69a47-947a-a478-e063-6394a90aa4682025-09-16WarningsExact identifier
ndc (package): 51316-217-01
ndc (product): 51316-217
ndc11 (package): 51316021701
spl id: 3ef5b095-2666-ab5c-e063-6294a90aca85
spl set id: 26a69a47-947a-a478-e063-6394a90aa468

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.