FDA.reportPublic FDA data

Preparation H

Product NDC
0573-2889
Requested package NDC
0573-2889-01
11-digit product format
005732889
Labeler code
0573
Product ID
0573-2889_d528363f-94d3-4234-8064-6eb50b198997
Type
HUMAN OTC DRUG
Nonproprietary name
witch hazel
Dosage form
AEROSOL, SPRAY
Route
TOPICAL
Labeler
GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Application
part346
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2021-04-12
Marketing end
0000-00-00
Substance
WITCH HAZEL
Active strength
200 mg/g
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage0573-28890573-2889-01DDiscontinued by firm2026-08-03

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0573-2889-010057328890177 g in 1 CANISTER (0573-2889-01) 77 g2021-04-120000-00-00NoNoCurrent