United States · FDA National Drug Code directory
Witch Hazel
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 41250-822_4b34762c-db2f-f8ba-e063-6394a90a273d
- Product NDC
- 41250-822
- Form
- LIQUID
- Composition / generic term
- WITCH HAZEL
- Labeler
- Meijer, Inc.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 19960315
- Source listing expiry
- 20271231
Source-listed ingredients
- WITCH HAZEL — 86 kg/100L
These values do not establish equivalence or a dose recommendation.
Packages
- .473 L in 1 BOTTLE, PLASTIC (41250-822-43) · 41250-822-43
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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