Mucosa Guifenesin
- Product NDC
- 54257-776
- 11-digit product format
- 542570776
- Labeler code
- 54257
- Product ID
- 54257-776_08bf8c82-76e6-440e-e063-6294a90af3d3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- GUAIFENESIN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Magno-Humphries, Inc.
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-01-24
- Substance
- GUAIFENESIN
- Active strength
- 400 mg/1
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Mucosa Guifenesin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GUAIFENESIN | 400 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 495W7451VQ |
| Rxcui | 359601 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 54257-776-21 | Mucosa Guifenesin | 60 in 1 BOTTLE | TABLET | 60 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 54257-776 | MUCOSA GUIFENESIN (GUAIFENESIN) TABLET [MAGNO-HUMPHRIES, INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20231030_9d22c208-d0ae-8b6a-e053-2995a90ab90a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 54257-776-21 | 54257077621 | 60 TABLET in 1 BOTTLE (54257-776-21) | 60 tablet | 2020-01-24 | 0000-00-00 | No | No | Current |