Home NDC 11673-822 Witch Hazel
Product NDC 11673-822
11-digit product format 116730822
Labeler code 11673
Product ID 11673-822_b7b722bf-281e-47f8-a0bb-19fe8d6f0ff3
Type HUMAN OTC DRUG
Nonproprietary name WITCH HAZEL
Dosage form LIQUID
Route TOPICAL
Labeler Target Corporation
Application part347
Marketing category OTC MONOGRAPH FINAL
Marketing start 1998-01-29
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 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 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 product product 11673-822 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 11673-822 11673-822-43 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11673-822 WITCH HAZEL LIQUID [TARGET CORPORATION] 16 Legacy NDC 20240726_62f15711-1f75-446d-bdd4-881b40e3eeab.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 11673-822-43 11673082243 473 L in 1 BOTTLE, PLASTIC (11673-822-43) 473 l 1998-01-29 0000-00-00 No No Current