Home NDC 48951-1409-5 Argentum 5X
Product NDC 48951-1409
Requested package NDC 48951-1409-5
11-digit product format 489511409
Labeler code 48951
Product ID 48951-1409_4bd30e47-c03a-06e8-e063-6294a90a8c4d
Type HUMAN OTC DRUG
Nonproprietary name Argentum 5X
Dosage form OINTMENT
Route TOPICAL
Labeler Uriel Pharmacy, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance COLLOIDAL SILVER
Active strength 5 [hp_X]/g
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 Argentum 5X
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength COLLOIDAL SILVER 5 [hp_X]/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3M4G523W1G Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-1409-5 Argentum 5X 60 g in 1 TUBE OINTMENT 60 1
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 Sample Exclude flag Status 48951-1409-5 48951140905 60 g in 1 TUBE (48951-1409-5) 60 g 2009-09-01 No No Current