Home NDC 87226-150 celimax PORE SKIN CLARIFYING DAILY SUNSCREEN
Product NDC 87226-150
11-digit product format 872260150
Labeler code 87226
Product ID 87226-150_5d21ba9c-417e-c742-e063-6294a90a7bb8
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form CREAM
Route TOPICAL
Labeler ABSORBLAB Co., Ltd
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-04-07
Substance HOMOSALATE; OCTISALATE; AVOBENZONE; OCTOCRYLENE
Active strength 6.8; 2.3; 1.4; 4.5 g/50mL; g/50mL; g/50mL; g/50mL
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 celimax PORE SKIN CLARIFYING DAILY SUNSCREEN
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 6.8 g/50mL OCTISALATE 2.3 g/50mL AVOBENZONE 1.4 g/50mL OCTOCRYLENE 4.5 g/50mL
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 87226-150-01 celimax PORE SKIN CLARIFYING DAILY SUNSCREEN 50 mL in 1 TUBE CREAM 50 2 87226-150-02 celimax PORE SKIN CLARIFYING DAILY SUNSCREEN 1 in 1 BOX CREAM 1 2
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 87226-150-01 87226015001 50 mL in 1 TUBE 50 ml Historical 87226-150-02 87226015002 1 TUBE in 1 BOX (87226-150-02) / 50 mL in 1 TUBE (87226-150-01) 1 tube 2026-04-07 No No Current