Home NDC 51316-922 CVS SPF 60 Face Sunscreen
Product NDC 51316-922
11-digit product format 513160922
Labeler code 51316
Product ID 51316-922_3f551b2b-f558-2245-e063-6294a90a736a
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form LIQUID
Route TOPICAL
Labeler CVS
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-01-17
Substance OCTISALATE; HOMOSALATE; OCTOCRYLENE; AVOBENZONE
Active strength 5; 10; 7; 3 g/100mL; g/100mL; g/100mL; g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base CVS SPF 60 Face Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 5 g/100mL HOMOSALATE 10 g/100mL OCTOCRYLENE 7 g/100mL AVOBENZONE 3 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51316-922-01 CVS SPF 60 Face Sunscreen 1 in 1 CARTON LIQUID 1 2 51316-922-01 CVS SPF 60 Face Sunscreen 50 mL in 1 BOTTLE LIQUID 50 2
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 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 51316-922-01 51316092201 1 BOTTLE in 1 CARTON (51316-922-01) / 50 mL in 1 BOTTLE 1 bottle 2025-01-17 No No Current