NDC 49892-0002-01 - Musco MXT
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
- 49892-0002
- Requested NDC
- 49892-0002-01
- Package NDCs from labels
- 49892-0002-1, 49892-0002-01
- Manufacturer
- Sandco International, Inc | Apotheca Company
- Effective date
- 2025-04-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Musco MXT - Sandco International, Inc | Apotheca Company | Sandco International, Inc | Apotheca Company | 2025-04-08 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49892-0002-1 | Musco MXT | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 49892-0002 | MUSCO MXT (ARALIA QUINQUEFOLIA, EPIPHEGUS VIRGINIANA, JACARANDA CAROBA, LACTICUM ACIDUM, HYDROCOTYLE ASIATICA, HYDROCYANICUM ACIDUM,) LIQUID [SANDCO INTERNATIONAL, INC] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250410_c35475c2-b138-4a4e-8e54-9cef93199b45.zip |
DailyMed Socrata Ingredients#
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.