Home NDC 87541-507 Dermasporin
Product NDC 87541-507
11-digit product format 875410507
Labeler code 87541
Product ID 87541-507_5738b40a-8261-9a9e-e063-6394a90a1f15
Type HUMAN OTC DRUG
Nonproprietary name Lanolin
Dosage form OINTMENT
Route TOPICAL
Labeler Marie's Original Formulas LLC
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-10
Substance LANOLIN
Active strength 3.96 g/14.2g
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 Dermasporin
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LANOLIN 3.96 g/14.2g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 7EV65EAW6H Internal UNII lookup
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 39 of 68 · 1,357 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87541-507-04 87541050704 14.2 g in 1 TUBE, WITH APPLICATOR (87541-507-04) 14.2 g 2026-07-10 No No Current