Mucus Relief
- Product NDC
- 46122-794
- 11-digit product format
- 461220794
- Labeler code
- 46122
- Product ID
- 46122-794_e85ab29d-ff4c-4781-8446-35399605ac8d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Amerisource Bergen
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-08-08
- 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 Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 46122-794-61 | Mucus Relief | 50 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 50 | | 5 |
| 46122-794-61 | Mucus Relief | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 46122-794 | MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [AMERISOURCE BERGEN] | 4 | Current NDC, 2 package rows | 20250323_087a3a0b-8d3f-45ed-8807-0af47b446cac.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 46122-794-61 | 46122079461 | 1 BOTTLE, PLASTIC in 1 CARTON (46122-794-61) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 2024-08-08 | No | No | Current |