Witch Hazel
- Product NDC
- 41250-383
- Requested package NDC
- 41250-383-06
- 11-digit product format
- 412500383
- Labeler code
- 41250
- Product ID
- 41250-383_f2048b24-4342-98ba-e053-2995a90a5e85
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Witch Hazel Spray
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Meijer Distribution Inc
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-03-01
- Marketing end
- 0000-00-00
- Substance
- WITCH HAZEL
- Active strength
- 146 g/170g
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 41250-383 | 41250-383-06 | D | Discontinued by firm | 2026-10-05 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 41250-383-06 | 41250038306 | 170 g in 1 CAN (41250-383-06) | 170 g | 2021-03-01 | 0000-00-00 | No | No | Current |