Argentum 12X

Product NDC: 48951-1321
11-digit product format: 489511321
Labeler code: 48951
Product ID: 48951-1321_94063fee-1d9b-11d4-e053-2995a90ab0d1
Type: HUMAN OTC DRUG
Nonproprietary name: Argentum 12X
Dosage form: LIQUID
Route: ORAL
Labeler: Uriel Pharmacy Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2009-09-01
Marketing end: 0000-00-00
Substance: SILVER
Active strength: 12 [hp_X]/mL
NDC exclude flag: No
Listing certified through: 2020-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
48951-1321-1	2025-01-30	C162847	48780-1	2cef2736-6c08-d83d-e063-dadaa90ab31f	Argentum 12X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-1321-1	Argentum 12X	60 mL in 1 BOTTLE, DROPPER	LIQUID	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-1321	ARGENTUM 12X LIQUID [URIEL PHARMACY INC.]	1	Legacy NDC, 1 package rows	20191004_94063fee-1d9a-11d4-e053-2995a90ab0d1.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-1321-1	48951132101	60 mL in 1 BOTTLE, DROPPER (48951-1321-1)	60 ml	2009-09-01	0000-00-00	No	No	Current