Arnica e rad. 12

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	48951-1135		I	Inactivated by FDA		2026-08-10
excluded package	package	48951-1135	48951-1135-2	I	Inactivated by FDA		2026-08-10

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-1135-2	Arnica e rad. 12	1350 in 1 BOTTLE, GLASS	PELLET	1350		2

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ARNICA MONTANA ROOT	ACTIVE INGREDIENT	MUE8Y11327	ARNICA E RAD. 12 PELLET [URIEL PHARMACY INC.]	1
ARNICA MONTANA ROOT	ACTIVE MOIETY	MUE8Y11327	ARNICA E RAD. 12 PELLET [URIEL PHARMACY INC.]	1
SUCROSE	INACTIVE INGREDIENT	C151H8M554	ARNICA E RAD. 12 PELLET [URIEL PHARMACY INC.]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-1135	ARNICA E RAD. 12 PELLET [URIEL PHARMACY INC.]	2	Legacy NDC, 1 package rows	20180531_e90a7cf5-6585-462c-b69c-bda0b83ab0a7.zip

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
MUE8Y11327	ARNICA MONTANA ROOT	ARNICA MONTANA ROOT

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-1135-2	48951113502	1350 PELLET in 1 BOTTLE, GLASS (48951-1135-2)	1350 pellet	2009-09-01	0000-00-00	No	No	Current