Home NDC 87236-019-04 Lanolin 50%
Product NDC 87236-019
Requested package NDC 87236-019-04
11-digit product format 872360019
Labeler code 87236
Product ID 87236-019_5c52af8e-7fad-8451-e063-6394a90a8908
Type HUMAN OTC DRUG
Nonproprietary name Lanolin
Dosage form CREAM
Route TOPICAL
Labeler Aldermed Inc.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-12-01
Substance LANOLIN
Active strength 50 g/100g
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 Lanolin 50%
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LANOLIN 50 g/100g
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 87236-019-04 Lanolin 50% 113 g in 1 TUBE CREAM 113 1
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 · 1,350 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87236-019-04 87236001904 113 g in 1 TUBE (87236-019-04) 113 g 2025-12-01 No No Current