NDC 79481-5330-01 - Mucus DM
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
- 79481-5330
- Requested NDC
- 79481-5330-01
- Package NDCs from labels
- 79481-5330-1, 79481-5330-01
- Manufacturer
- Meijer Distribution, Inc. | LNK International, Inc.
- Effective date
- 2026-03-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Meijer 44-533 New | Meijer Distribution, Inc. | LNK International, Inc. | 2026-03-06 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79481-5330-1 | Mucus DM | 60 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 60 | 3 | |
| 79481-5330-1 | Mucus DM | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 79481-5330 | MUCUS DM (DEXTROMETHORPHAN HBR, GUAIFENESIN) TABLET, FILM COATED [MEIJER DISTRIBUTION, INC.] | 2 | Current NDC, 2 package rows | 20250322_87cf4f25-b0e9-4f8b-bde3-0d0f26e2120e.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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.