FDA.reportPublic FDA data

Witch Hazel

Product NDC
68016-822
11-digit product format
680160822
Labeler code
68016
Product ID
68016-822_6b6037ea-0440-45c1-acf3-d5d56d6c0eea
Type
HUMAN OTC DRUG
Nonproprietary name
WITCH HAZEL
Dosage form
LIQUID
Route
TOPICAL
Labeler
Pharmacy Vlaue Alliance LLC
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2003-08-15
Marketing end
0000-00-00
Substance
WITCH HAZEL
Active strength
842 mg/mL
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct68016-822DDiscontinued by firm2026-10-05
excluded packagepackage68016-82268016-822-43DDiscontinued 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 productproduct68016-822DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage68016-82268016-822-43DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…

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 [CHAIN DRUG CONSORTIUM, LLC]1
WITCH HAZELACTIVE MOIETY101I4J0U34WITCH HAZEL LIQUID [CHAIN DRUG CONSORTIUM, LLC]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MWITCH HAZEL LIQUID [CHAIN DRUG CONSORTIUM, LLC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68016-822WITCH HAZEL LIQUID [PHARMACY VLAUE ALLIANCE LLC]15Legacy NDC20240928_161de71d-c919-4e12-80a4-dc4e394f9ff7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68016-822-4368016082243473 mL in 1 BOTTLE, PLASTIC (68016-822-43) 473 ml2003-08-150000-00-00NoNoCurrent