Home NDC 51316-167 CVS SPF 70 Sport Face Sunscreen
Product NDC 51316-167
11-digit product format 513160167
Labeler code 51316
Product ID 51316-167_4d28043c-9f64-6fe1-e063-6394a90ac66c
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form LOTION
Route TOPICAL
Labeler CVS
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-01-28
Substance OCTISALATE; HOMOSALATE; OCTOCRYLENE; AVOBENZONE
Active strength 5; 15; 10; 3 g/100mL; g/100mL; g/100mL; g/100mL
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 SPF 70 Sport Face Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 5 g/100mL HOMOSALATE 15 g/100mL OCTOCRYLENE 10 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 51316-167-02 CVS SPF 70 Sport Face Sunscreen 74 mL in 1 BOTTLE LOTION 74 3
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 81 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 51316-167-02 51316016702 74 mL in 1 BOTTLE (51316-167-02) 74 ml 2025-01-28 No No Current