Aurum Prunus

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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	48951-1204	48951-1204-2	I	Inactivated by FDA		2026-10-05

Adverse event summaries are temporarily unavailable. Other product information remains available.

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-1204-2	Aurum Prunus	1350 in 1 BOTTLE, GLASS	PELLET	1350		5

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
GOLD	ACTIVE INGREDIENT	79Y1949PYO	AURUM PRUNUS PELLET [URIEL PHARMACY INC.]	1
SLOE	ACTIVE INGREDIENT	3MLB4858X7	AURUM PRUNUS PELLET [URIEL PHARMACY INC.]	1
GOLD	ACTIVE MOIETY	79Y1949PYO	AURUM PRUNUS PELLET [URIEL PHARMACY INC.]	1
SLOE	ACTIVE MOIETY	3MLB4858X7	AURUM PRUNUS PELLET [URIEL PHARMACY INC.]	1
SUCROSE	INACTIVE INGREDIENT	C151H8M554	AURUM PRUNUS PELLET [URIEL PHARMACY INC.]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-1204	AURUM PRUNUS PELLET [URIEL PHARMACY INC.]	5	Legacy NDC, 1 package rows	20241116_103f19d2-8ca4-44dc-9c09-d718af07fc91.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3MLB4858X7	SLOE		SLOE
79Y1949PYO	GOLD	7440-57-5	GOLD

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-1204-2	48951120402	1350 PELLET in 1 BOTTLE, GLASS (48951-1204-2)	1350 pellet	2009-09-01	0000-00-00	No	No	Current