Witch Hazel

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

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	0869-0822		D	Discontinued by firm		2026-07-31
excluded package	package	0869-0822	0869-0822-43	D	Discontinued by firm		2026-07-31

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0869-0822-43	2022-09-13	C162847	48780-1	e4f33bdf-a0fe-d8a0-e053-dadaa90a6e4e	Witch Hazel 822.001/822AA
0869-0822-43	2022-07-29	C162847	48780-1	e4f33bdf-a0fe-d8a0-e053-dadaa90a6e4e	Witch Hazel 822.001/822AA

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
WITCH HAZEL	ACTIVE INGREDIENT	101I4J0U34	WITCH HAZEL LIQUID [VI-JON]	1
WITCH HAZEL	ACTIVE MOIETY	101I4J0U34	WITCH HAZEL LIQUID [VI-JON]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	WITCH HAZEL LIQUID [VI-JON]	1

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
101I4J0U34	WITCH HAZEL	WITCH HAZEL

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0869-0822-43	00869082243	473 L in 1 BOTTLE, PLASTIC (0869-0822-43)	473 l	1998-01-29	0000-00-00	No	No	Current