Home NDC 87501-002 BaseLife Clear UV Defense Sunscreen
Product NDC 87501-002
11-digit product format 875010002
Labeler code 87501
Product ID 87501-002_56a386d1-0c6a-c666-e063-6294a90a10ba
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form CREAM
Route TOPICAL
Labeler Wintech America, Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-14
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength 30; 100; 50; 50 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 BaseLife Clear UV Defense Sunscreen
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 50 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.
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 87501-002-02 87501000202 1 TUBE in 1 CARTON (87501-002-02) / 50 mL in 1 TUBE (87501-002-01) 1 tube 2026-07-14 No No Current