FDA.reportPublic FDA data

Witch Hazel

Product NDC
41190-822
Requested package NDC
41190-822-43
11-digit product format
411900822
Labeler code
41190
Product ID
41190-822_0a2708e4-f630-4984-8201-b1a28cd15ca9
Type
HUMAN OTC DRUG
Nonproprietary name
WITCH HAZEL
Dosage form
LIQUID
Route
TOPICAL
Labeler
Wakefern Food Corp
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
1989-07-15
Marketing end
0000-00-00
Substance
WITCH HAZEL
Active strength
86 kg/100L
NDC exclude flag
No
Listing certified through
2023-12-31
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
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage41190-82241190-822-43DDiscontinued by firm2026-10-05

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 · 2 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage41190-82241190-822-43DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage41190-82241190-822-43DDiscontinued by firmexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
WITCH HAZELACTIVE INGREDIENT101I4J0U34WITCH HAZEL LIQUID [WAKEFERN FOOD CORP]1
WITCH HAZELACTIVE MOIETY101I4J0U34WITCH HAZEL LIQUID [WAKEFERN FOOD CORP]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MWITCH HAZEL LIQUID [WAKEFERN FOOD CORP]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41190-822WITCH HAZEL LIQUID [WAKEFERN FOOD CORP]16Legacy NDC20240929_22276aa9-1cc1-46bf-a13d-83bbb90cd545.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
41190-822-4341190082243.473 L in 1 BOTTLE, PLASTIC (41190-822-43) 1989-07-150000-00-00NoNoCurrent