Witch Hazel

Product NDC: 50804-390
Requested package NDC: 50804-390-16
11-digit product format: 508040390
Labeler code: 50804
Product ID: 50804-390_06aa3f5f-2380-4a6e-af82-98360ac811ba
Type: HUMAN OTC DRUG
Nonproprietary name: Witch hazel
Dosage form: LIQUID
Route: TOPICAL
Labeler: Good Sense (Geiss, Destin & Dunn, Inc.)
Application: part347
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2016-09-30
Marketing end: 0000-00-00
Substance: WITCH HAZEL
Active strength: 842 mg/mL
NDC exclude flag: No
Listing certified through: 2020-12-31
Current FDA listing: Historical FDA.report record

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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	50804-390	50804-390-16	D	Discontinued by firm		2026-10-16

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 1 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	50804-390	50804-390-16	D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
50804-390-16	2023-02-11	C162847	48780-1	f386c649-9a19-0266-e053-dadaa90a7c1a	Drug Facts
50804-390-16	2023-01-30	C162847	48780-1	f386c649-9a19-0266-e053-dadaa90a7c1a	Drug Facts

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50804-390	WITCH HAZEL LIQUID [GOOD SENSE (GEISS, DESTIN & DUNN, INC.)]	3	Legacy NDC	20230212_a5aab89b-5314-417f-8bd7-19c7de8ce18c.zip

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

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
50804-390-16	50804039016	473 mL in 1 BOTTLE, PLASTIC (50804-390-16)	473 ml	2016-09-30	0000-00-00	No	No	Current