Argentum 6

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	48951-1085		I	Inactivated by FDA		2026-08-11
excluded package	package	48951-1085	48951-1085-3	I	Inactivated by FDA		2026-08-11

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-1085-3	Argentum 6	60 mL in 1 BOTTLE, DROPPER	LIQUID	60		3

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
SILVER	ACTIVE INGREDIENT	3M4G523W1G	ARGENTUM 6 LIQUID [URIEL PHARMACY INC.]	1
SILVER	ACTIVE MOIETY	3M4G523W1G	ARGENTUM 6 LIQUID [URIEL PHARMACY INC.]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	ARGENTUM 6 LIQUID [URIEL PHARMACY INC.]	1
LACTOSE	INACTIVE INGREDIENT	J2B2A4N98G	ARGENTUM 6 LIQUID [URIEL PHARMACY INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	ARGENTUM 6 LIQUID [URIEL PHARMACY INC.]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-1085	ARGENTUM 6 LIQUID [URIEL PHARMACY INC.]	3	Legacy NDC, 1 package rows	20241215_327f6284-1cd1-41f7-b139-f45c57ee1bcf.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3M4G523W1G	SILVER	7440-22-4	SILVER

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-1085-3	48951108503	60 mL in 1 BOTTLE, DROPPER (48951-1085-3)	60 ml	2009-09-01	0000-00-00	No	No	Current