Home NDC 44911-0379 Argentum Nitricum
Product NDC 44911-0379
11-digit product format 449110379
Labeler code 44911
Product ID 44911-0379_eee7a9ff-4e00-4c5b-8e00-8f803acb6558
Type HUMAN OTC DRUG
Nonproprietary name Argentum Nitricum
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2016-08-16
Marketing end 2026-08-05
Substance SILVER NITRATE
Active strength 200 [hp_C]/mL
NDC exclude flag No
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Argentum Nitricum Active Ingredients# Ingredient, Strength table Ingredient Strength SILVER NITRATE 200 [hp_C]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 95IT3W8JZE Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 44911-0379-1 Argentum Nitricum 30 mL in 1 BOTTLE, DROPPER LIQUID 30 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 44911-0379 ARGENTUM NITRICUM LIQUID [ENERGIQUE, INC.] 3 Current NDC, Legacy NDC, 1 package rows 20220630_7e40134a-b3ce-495f-9f5d-f1d0f2856451.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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 44911-0379-1 44911037901 30 mL in 1 BOTTLE, DROPPER (44911-0379-1) 30 ml 2016-08-16 2026-08-05 No No Current