NDC 81825-0010-01 - Stress
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
- 81825-0010
- Requested NDC
- 81825-0010-01
- Package NDCs from labels
- 81825-0010-1, 81825-0010-01
- Manufacturer
- Zorex International | OHM Pharma, Inc
- Effective date
- 2018-12-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Stress - Zorex International | OHM Pharma, Inc | Zorex International | OHM Pharma, Inc | 2018-12-21 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81825-0010-1 | Stress | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 81825-0010 | STRESS (ARALIA QUIN, PASSIFLORA, SCUTELLARIA, VALERIANA, ARSENICUM ALB, AUR MET, CALC CARB, COFFEA CRUDA, IGNATIA, KALI PHOS, LYCOPUS, PHOSPHORUS, STAPHYSAGRIA) LIQUID [ZOREX INTERNATIONAL] | 1 | Current NDC, 1 package rows | 20230420_d0527396-7b7f-4252-be0f-d3aa74c25e0e.zip |
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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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.