Medi-Pads
- Product NDC
- 0904-5059
- 11-digit product format
- 009045059
- Labeler code
- 0904
- Product ID
- 0904-5059_d19b8c40-5202-4ce5-835c-3aa9f3f6dcdb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- witch hazel
- Dosage form
- SOLUTION
- Route
- RECTAL; TOPICAL
- Labeler
- Major Pharmaceuticals
- Application
- part346
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2011-10-25
- Marketing end
- 2020-12-31
- Substance
- WITCH HAZEL
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 0904-5059 | D | Discontinued by firm | 2026-07-31 | ||
| excluded package | package | 0904-5059 | 0904-5059-60 | D | Discontinued by firm | 2026-07-31 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0904-5059-60 | EA - Each | 0904-5059 | 1a46e5dd-8937-4df2-8baf-cdef69eb95b7 | 1 | 2012-07-24 |