Home NDC 0220-0466 Argentum nitricum
Product NDC 0220-0466
11-digit product format 002200466
Labeler code 0220
Product ID 0220-0466_3f7de6b2-8b86-c117-e063-6294a90acfcb
Type HUMAN OTC DRUG
Nonproprietary name SILVER NITRATE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance SILVER NITRATE
Active strength 200 [kp_C]/200[kp_C]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Argentum nitricum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SILVER NITRATE 200 [kp_C]/200[kp_C]
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 0220-0466-41 Argentum nitricum 200 [kp_C] in 1 TUBE PELLET 200 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-0466 ARGENTUM NITRICUM (SILVER NITRATE ) PELLET [BOIRON] 3 Current NDC, Legacy NDC, 1 package rows 20230222_84edf684-c38c-3f30-e053-2a91aa0a3772.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 Marketing start Marketing end Sample Exclude flag Status 0220-0466-41 00220046641 200 [kp_C] in 1 TUBE (0220-0466-41) 1983-03-03 0000-00-00 No No Current