Home NDC 87767-001 MORANDIPARK PANTHENOL ULTRA LIGHT SUNSCREEN
Product NDC 87767-001
11-digit product format 877670001
Labeler code 87767
Product ID 87767-001_54fbed51-4f40-64be-e063-6294a90a1a0b
Type HUMAN OTC DRUG
Nonproprietary name Homosalate, Octocrylene, Octisalate, Avobenzone
Dosage form CREAM
Route TOPICAL
Labeler BRAND GENOME CO., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-05-22
Substance HOMOSALATE; OCTISALATE; OCTOCRYLENE; AVOBENZONE
Active strength 13.5; 4.5; 9; 2.7 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 MORANDIPARK PANTHENOL ULTRA LIGHT SUNSCREEN
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 13.5 g/100mL OCTISALATE 4.5 g/100mL OCTOCRYLENE 9 g/100mL AVOBENZONE 2.7 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.
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 87767-001-01 87767000101 1 CONTAINER in 1 BOX (87767-001-01) / 40 mL in 1 CONTAINER 1 container 2026-06-12 No No Current