Home NDC 81507-003 Dermeleve
Product NDC 81507-003
11-digit product format 815070003
Labeler code 81507
Product ID 81507-003_5d19622c-b21d-3994-e063-6394a90a960b
Type HUMAN OTC DRUG
Nonproprietary name Aluminum Acetate
Dosage form CREAM
Route TOPICAL
Labeler Advanced Derm Solutions LLC
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-02-04
Substance ALUMINUM ACETATE
Active strength .2 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 Dermeleve
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM ACETATE .2 g/100g
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81507-003-01 Dermeleve 120 g in 1 TUBE CREAM 120 7 81507-003-02 Dermeleve 113 g in 1 TUBE CREAM 113 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81507-003 DERMELEVE (ALUMINUM ACETATE) CREAM [ADVANCED DERM SOLUTIONS LLC] 5 Current NDC, Legacy NDC, 2 package rows 20241018_5dd4c952-8880-4c06-9c09-20c6a3cdd0f5.zip
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 59 of 68 · 1,357 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 81507-003-01 81507000301 120 g in 1 TUBE (81507-003-01) 120 g 2022-02-04 0000-00-00 No No Current 81507-003-02 81507000302 113 g in 1 TUBE (81507-003-02) 113 g 2025-05-28 No No Current