Home NDC 41250-822 Witch Hazel
Product NDC 41250-822
11-digit product format 412500822
Labeler code 41250
Product ID 41250-822_4b34762c-db2f-f8ba-e063-6394a90a273d
Type HUMAN OTC DRUG
Nonproprietary name WITCH HAZEL
Dosage form LIQUID
Route TOPICAL
Labeler Meijer, Inc.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 1996-03-15
Substance WITCH HAZEL
Active strength 86 kg/100L
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 package package 41250-822 41250-822-99 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 41250-822 41250-822-99 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Witch Hazel
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength WITCH HAZEL 86 kg/100L
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 101I4J0U34 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 200295 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 41250-822-43 Witch Hazel 0.473 L in 1 BOTTLE, PLASTIC LIQUID 0.473 20 41250-822-99 Witch Hazel 0.236 L in 1 BOTTLE, PUMP LIQUID 0.236 20
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41250-822 WITCH HAZEL LIQUID [MEIJER DISTRIBUTION, INC] 18 Current NDC, Legacy NDC, 2 package rows 20241114_13e4aece-5b91-4f89-a912-540bf170a8d1.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 55 of 68 · 1,357 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 41250-822-43 41250082243 .473 L in 1 BOTTLE, PLASTIC (41250-822-43) 1996-03-15 0000-00-00 No No Current 41250-822-99 41250082299 .236 L in 1 BOTTLE, PUMP (41250-822-99) 1996-03-15 0000-00-00 No No Current