Arnica Bryonia Special Order

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	48951-1288		I	Inactivated by FDA		2026-10-05
excluded package	package	48951-1288	48951-1288-3	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
48951-1288-3	Arnica Bryonia Special Order	60 mL in 1 BOTTLE, DROPPER	LIQUID	60		1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-1288	ARNICA BRYONIA SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]	1	Legacy NDC, 1 package rows	20180515_6b3ec25a-65bb-de80-e053-2991aa0aa70d.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
O80TY208ZW	ARNICA MONTANA	8057-65-6	ARNICA MONTANA
T7J046YI2B	BRYONIA ALBA ROOT		BRYONIA ALBA ROOT
U0NQ8555JD	ACONITUM NAPELLUS		ACONITUM NAPELLUS

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-1288-3	48951128803	60 mL in 1 BOTTLE, DROPPER (48951-1288-3)	60 ml	2009-09-01	0000-00-00	No	No	Current