Home NDC 84281-893 Summer Face Sunscreen SPF 50
Product NDC 84281-893
11-digit product format 842810893
Labeler code 84281
Product ID 84281-893_407e0bda-0096-451d-e063-6294a90abcf2
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form LIQUID
Route TOPICAL
Labeler SUMMER GELEE LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-09-04
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength 30; 100; 50; 75 mg/mL; mg/mL; mg/mL; mg/mL
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 Summer Face Sunscreen SPF 50
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/mL HOMOSALATE 100 mg/mL OCTISALATE 50 mg/mL OCTOCRYLENE 75 mg/mL
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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 84281-893-00 Summer Face Sunscreen SPF 50 79.78 mL in 1 TUBE LIQUID 79.78 1
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 84281-893-00 84281089300 79.78 mL in 1 TUBE (84281-893-00) 79.78 ml 2025-09-04 No No Current