CVS Arnica

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	66902-778		D	Discontinued by firm		2026-10-28
excluded package	package	66902-778	66902-778-26	D	Discontinued by firm		2026-10-28

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
66902-778-26	CVS Arnica	73 g in 1 TUBE	GEL	73		2
66902-778-26	CVS Arnica	1 in 1 CARTON	GEL	1		2

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
66902-778	CVS ARNICA (ARNICA MONTANA FLOWER) GEL [NATURAL ESSENTIALS, INC.]	2	Legacy NDC, 2 package rows	20241004_e49ae317-a03d-4576-ba27-f661469584ed.zip

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
OZ0E5Y15PZ	ARNICA MONTANA FLOWER	ARNICA MONTANA FLOWER

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
66902-778-26	66902077826	1 TUBE in 1 CARTON (66902-778-26) > 73 g in 1 TUBE	1 tube	2021-01-27	0000-00-00	No	No	Current