Crataegus e fol. et. fruct. 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	48951-3212		I	Inactivated by FDA		2026-08-10
excluded package	package	48951-3212	48951-3212-3	I	Inactivated by FDA		2026-08-10

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-3212-3	Crataegus e fol. et. fruct. 1% 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
48951-3212	CRATAEGUS E FOL. ET. FRUCT. 1% SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]	1	Legacy NDC, 1 package rows	20180504_6b64e2f0-0afc-200d-e053-2991aa0a220c.zip

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
6OM09RPY36	HAWTHORN LEAF WITH FLOWER	HAWTHORN LEAF WITH FLOWER

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-3212-3	48951321203	60 mL in 1 BOTTLE, DROPPER (48951-3212-3)	60 ml	2009-09-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Crataegus e fol. et. fruct. 1% Special Order	Uriel Pharmacy Inc.	2018-05-04	HUMAN OTC DRUG LABEL	1