Home NDC 87236-010 Hydrating
Product NDC 87236-010
11-digit product format 872360010
Labeler code 87236
Product ID 87236-010_516c8466-5860-05cb-e063-6394a90a9889
Type HUMAN OTC DRUG
Nonproprietary name Petrolatum
Dosage form OINTMENT
Route TOPICAL
Labeler Aldermed Inc.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-12-01
Substance PETROLATUM
Active strength 41 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 Hydrating
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PETROLATUM 41 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4T6H12BN9U Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 725145 Internal RxNorm lookup
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 87236-010-37 Hydrating 106 g in 1 TUBE CREAM 106 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 28 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 87236-010-37 87236001037 106 g in 1 TUBE (87236-010-37) 106 g 2025-12-01 No No Current