Home NDC 87669-963 Poth Clear Gel Sunscreen SPF 50
Product NDC 87669-963
11-digit product format 876690963
Labeler code 87669
Product ID 87669-963_5123e244-ac63-ebf1-e063-6394a90a14e3
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form GEL
Route TOPICAL
Labeler Poth LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-04-14
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength 30; 100; 50; 100 mg/mL; mg/mL; mg/mL; mg/mL
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 Poth Clear Gel Sunscreen SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/mL HOMOSALATE 100 mg/mL OCTISALATE 50 mg/mL OCTOCRYLENE 100 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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 87669-963-00 Poth Clear Gel Sunscreen SPF 50 59 mL in 1 BOTTLE GEL 59 1 87669-963-00 Poth Clear Gel Sunscreen SPF 50 1 in 1 BOX GEL 1 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 87669-963-00 87669096300 1 BOTTLE in 1 BOX (87669-963-00) / 59 mL in 1 BOTTLE 1 bottle 2024-04-14 No No Current