Home NDC 87807-001 SPF 50 plus Sunscreen
Product NDC 87807-001
11-digit product format 878070001
Labeler code 87807
Product ID 87807-001_55a25daf-4da3-7367-e063-6394a90a5b33
Type HUMAN OTC DRUG
Nonproprietary name TITANIUM DIOXIDE and ZINC OXIDE
Dosage form STICK
Route TOPICAL
Labeler Theravita LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-02
Substance OCTOCRYLENE; OCTISALATE; OCTINOXATE; AVOBENZONE
Active strength 80; 50; 75; 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 SPF 50 plus Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTOCRYLENE 80 mg/g OCTISALATE 50 mg/g OCTINOXATE 75 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 87807-001-01 87807000101 1 BOTTLE in 1 BOX (87807-001-01) / 15 g in 1 BOTTLE 1 bottle 2026-07-02 No No Current