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	48951-7180		I	Inactivated by FDA		2026-09-14
excluded package	package	48951-7180	48951-7180-5	I	Inactivated by FDA		2026-09-14

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-7180-5	Oxalis 20	60 g in 1 TUBE	GEL	60		2

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-7180	OXALIS 20 GEL [URIEL PHARMACY INC.]	2	Legacy NDC, 1 package rows	20190213_81404737-8f0f-6dce-e053-2a91aa0a1478.zip

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
U1W3U02EW0	OXALIS ACETOSELLA LEAF	OXALIS ACETOSELLA LEAF

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-7180-5	48951718005	60 g in 1 TUBE (48951-7180-5)	60 g	2009-09-01	0000-00-00	No	No	Current