Home NDC 51141-0701 Derma B Everyday Fit Sunscreen SPF 50
Product NDC 51141-0701
11-digit product format 511410701
Labeler code 51141
Product ID 51141-0701_4a0024d0-7a49-7495-e063-6394a90a9371
Type HUMAN OTC DRUG
Nonproprietary name AVOBEZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form LOTION
Route TOPICAL
Labeler NeoPharm Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-12-15
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength 30; 95; 45; 60 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 Derma B Everyday Fit Sunscreen SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/mL HOMOSALATE 95 mg/mL OCTISALATE 45 mg/mL OCTOCRYLENE 60 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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51141-0701-5 Derma B Everyday Fit Sunscreen SPF 50 50 mL in 1 TUBE LOTION 50 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 128 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 51141-0701-5 51141070105 50 mL in 1 TUBE (51141-0701-5) 50 ml 2025-12-15 No No Current