Petasites e rad. 1 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	48951-8018		I	Inactivated by FDA		2026-09-14
excluded package	package	48951-8018	48951-8018-3	I	Inactivated by FDA		2026-09-14

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-8018-3	Petasites e rad. 1 Special Order	60 mL in 1 BOTTLE, DROPPER	LIQUID	60		2

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
PETASITES HYBRIDUS ROOT	ACTIVE INGREDIENT	97S2809V5R	PETASITES E RAD. 1 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]	1
PETASITES HYBRIDUS ROOT	ACTIVE MOIETY	97S2809V5R	PETASITES E RAD. 1 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	PETASITES E RAD. 1 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	PETASITES E RAD. 1 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-8018	PETASITES E RAD. 1 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]	2	Legacy NDC, 1 package rows	20180430_2d0f5e23-092d-45d9-a6b6-981ae8256a25.zip

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
97S2809V5R	PETASITES HYBRIDUS ROOT	PETASITES HYBRIDUS ROOT

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-8018-3	48951801803	60 mL in 1 BOTTLE, DROPPER (48951-8018-3)	60 ml	2009-09-01	0000-00-00	No	No	Current