NDC 81507-005 - Dermeleve

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
81507-005
Package NDCs from labels
81507-005-01, 81507-005-02
Manufacturer
Advanced Derm Solutions LLC
Effective date
2024-08-16
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Dermeleve - Advanced Derm Solutions LLCAdvanced Derm Solutions LLC2024-08-16HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81507-005-01Dermeleve1 in 1 BOXCREAM11
81507-005-01Dermeleve60 g in 1 TUBECREAM601
81507-005-02Dermeleve120 g in 1 TUBECREAM1201
81507-005-02Dermeleve1 in 1 BOXCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81507-005DERMELEVE (PRAMOXINE HYDROCHLORIDE) CREAM [ADVANCED DERM SOLUTIONS LLC]14 package rows20241102_5f448090-642c-4c36-a53d-2aab9c1398b4.zip