FDA.reportPublic FDA data

NDC 76472-1126-01 - Argentum Nitricum

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
76472-1126
Requested NDC
76472-1126-01
Package NDCs from labels
76472-1126-1, 76472-1126-01
Manufacturer
SEVENE USA
Effective date
2024-01-23
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Argentum Nitricum - SEVENE USASEVENE USA2024-01-23HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76472-1126-1Argentum Nitricum80 in 1 CYLINDERPELLET8021

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76472-1126ARGENTUM NITRICUM (SILVER NITRATE) PELLET [SEVENE USA]21Current NDC, Legacy NDC, 1 package rows20240127_b57e61fc-5aaf-4fd9-a617-aa764b652966.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SILVER NITRATEACTIVE INGREDIENT95IT3W8JZEARGENTUM NITRICUM (SILVER NITRATE) PELLET [BRANDSTORM HBC]2
SILVER CATIONACTIVE MOIETY57N7B0K90AARGENTUM NITRICUM (SILVER NITRATE) PELLET [BRANDSTORM HBC]2
lactoseINACTIVE INGREDIENTJ2B2A4N98GARGENTUM NITRICUM (SILVER NITRATE) PELLET [BRANDSTORM HBC]2
sucroseINACTIVE INGREDIENTC151H8M554ARGENTUM NITRICUM (SILVER NITRATE) PELLET [BRANDSTORM HBC]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 15 of 15 · 281 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Silver NitrateSILVER NITRATETeva Pharmaceuticals USA, Inc.6956c883-fc1b-49be-97bc-e642e0aa907d2016-02-01Exact identifier
unii: 95IT3W8JZE

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.