United States · FDA National Drug Code directory
AER Pre-moistened Witch Hazel Pad
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
- 50289-3250_2baae3c5-a04e-c51e-e063-6394a90a81c3
- Product NDC
- 50289-3250
- Form
- SOLUTION
- Composition / generic term
- Witch Hazel
- Labeler
- Birchwood Laboratories LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20180628
- Source listing expiry
- 20261231
Source-listed ingredients
- WITCH HAZEL — 500 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 40 APPLICATOR in 1 JAR (50289-3250-1) / 2.8 mL in 1 APPLICATOR · 50289-3250-1
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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