Mucus Relief
- Product NDC
- 55681-311
- 11-digit product format
- 556810311
- Labeler code
- 55681
- Product ID
- 55681-311_4dc83923-e74d-3466-e063-6294a90a4f7d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin 400 mg
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- TWIN MED LLC
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-07-01
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Mucus Relief
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GUAIFENESIN | 400 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 495W7451VQ |
| Rxcui | 359601 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55681-311-03 | Mucus Relief | 300 in 1 BOTTLE | TABLET | 300 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55681-311 | MUCUS RELIEF (GUAIFENESIN 400 MG) TABLET [TWIN MED LLC] | 3 | Current NDC, Legacy NDC, 1 package rows | 20241030_e31bd69f-97ab-9d99-e053-2995a90a580e.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 |
|---|
| 55681-311-03 | 55681031103 | 300 TABLET in 1 BOTTLE (55681-311-03) | 300 tablet | 2022-07-01 | 0000-00-00 | No | No | Current |