Home NDC 81507-004 Dermeleve Anti Itch Scalp Serum
Product NDC 81507-004
11-digit product format 815070004
Labeler code 81507
Product ID 81507-004_5d1968ca-9ba6-437e-e063-6294a90a9dd6
Type HUMAN OTC DRUG
Nonproprietary name Aluminum Acetate
Dosage form SOLUTION
Route TOPICAL
Labeler Advanced Derm Solutions LLC
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-06-02
Substance ALUMINUM ACETATE
Active strength .2 g/100mL
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 Anti Itch Scalp Serum
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM ACETATE .2 g/100mL
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81507-004-01 Dermeleve Anti Itch Scalp Serum 89 mL in 1 BOTTLE SOLUTION 89 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81507-004 DERMELEVE ANTI ITCH SCALP SERUM (ALUMINUM ACETATE) SOLUTION [ADVANCED DERM SOLUTIONS LLC] 4 Current NDC, 1 package rows 20241109_c53e075e-b9cb-4434-a38d-2cf3dae0b438.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 39 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 Sample Exclude flag Status 81507-004-01 81507000401 89 mL in 1 BOTTLE (81507-004-01) 89 ml 2023-06-02 No No Current