Home NDC 0573-2889 Preparation H
Product NDC 0573-2889
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 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 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 0573-2889-01 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 0573-2889-01 f5e01cc5f278…a2eaf40c39c3…
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 0573-2889-01 00573288901 77 g in 1 CANISTER (0573-2889-01) 77 g 2021-04-12 0000-00-00 No No Current