NDC 72839-413 - Dermatool Hemorrhoidal
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 72839-413
- Package NDCs from labels
- 72839-413-01
- Manufacturer
- Derma Care Research Labs, LLC
- Effective date
- 2024-12-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Dermatool Hemorrhoidal - Derma Care Research Labs, LLC | Derma Care Research Labs, LLC | 2024-12-19 | HUMAN OTC DRUG LABEL |
DailyMed Dashboard NDC Coverage#
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.
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| Tussin Multi Symptom Cold CF | DEXTROMETHORPHAN HBR GUAIFENESIN PHENYLEPHRINE HCL | QUALITY CHOICE (Chain Drug Marketing Association) | b225e897-5728-4519-b727-c0f361c75976 | 2026-01-07 | Warnings | 04JA59TNSJ |
| Healthwise Anorectal Pain Relief | LIDOCAINE 5% | Veridian Healthcare | 19c24e1b-a31b-478b-a48b-c39bb4753ca7 | 2026-01-06 | Warnings | 98PI200987 |
| Proctozone-G | GLYCERIN | Rising Pharma Holdings, Inc. | 8a5c8ad5-3619-4971-967d-165270a20bc8 | 2026-01-06 | Warnings | PDC6A3C0OX |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.