Arnica e pl. tota 6X

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	48951-8378		I	Inactivated by FDA		2026-10-05
excluded package	package	48951-8378	48951-8378-3	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
48951-8378-3	Arnica e pl. tota 6X	60 mL in 1 BOTTLE, DROPPER	LIQUID	60		2

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-8378	ARNICA E PL. TOTA 6X LIQUID [URIEL PHARMACY INC.]	2	Legacy NDC, 1 package rows	20240120_c70507f3-b220-66e7-e053-2a95a90adeae.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
O80TY208ZW	ARNICA MONTANA	8057-65-6	ARNICA MONTANA

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-8378-3	48951837803	60 mL in 1 BOTTLE, DROPPER (48951-8378-3)	60 ml	2009-09-01	0000-00-00	No	No	Current