Oxalis 20%

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	48951-7198		I	Inactivated by FDA		2026-08-07
excluded package	package	48951-7198	48951-7198-5	I	Inactivated by FDA		2026-08-07

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-7198-5	Oxalis 20%	60 g in 1 TUBE	CREAM	60		2

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-7198	OXALIS 20% CREAM [URIEL PHARMACY INC.]	2	Legacy NDC, 1 package rows	20240514_cf32aa91-9c58-1e02-e053-2a95a90ab611.zip

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
3STW243384	OXALIS STRICTA WHOLE	OXALIS STRICTA WHOLE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-7198-5	48951719805	60 g in 1 TUBE (48951-7198-5)	60 g	2009-09-01	0000-00-00	No	No	Current