Home NDC 51316-974 CVS 70 Daily Clear Sunscreen
Product NDC 51316-974
11-digit product format 513160974
Labeler code 51316
Product ID 51316-974_54f258fa-4556-6d66-e063-6394a90ace02
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form SPRAY
Route TOPICAL
Labeler CVS PHARMACY
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-03-01
Substance OCTISALATE; OCTOCRYLENE; HOMOSALATE; AVOBENZONE
Active strength 50; 100; 150; 30 mg/g; mg/g; mg/g; mg/g
NDC exclude flag No
Listing certified through 2027-12-31
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 70 Daily Clear Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 50 mg/g OCTOCRYLENE 100 mg/g HOMOSALATE 150 mg/g AVOBENZONE 30 mg/g
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.
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 51316-974-37 51316097437 156 g in 1 CAN (51316-974-37) 156 g 2026-03-01 No No Current