Mucus Relief
- Product NDC
- 50804-857
- 11-digit product format
- 508040857
- Labeler code
- 50804
- Product ID
- 50804-857_3aa57e05-8ba4-488a-aa9d-38252490625a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Good Sense (Geiss, Destin & Dunn, Inc.)
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-02-28
- Marketing end
- 2026-06-30
- Substance
- GUAIFENESIN
- Active strength
- 400 mg/1
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Mucus Relief
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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50804-857-30 | Mucus Relief | 1 in 1 BOX | TABLET | 1 | | 4 |
| 50804-857-30 | Mucus Relief | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50804-857 | MUCUS RELIEF (GUAIFENESIN) TABLET [GOOD SENSE (GEISS, DESTIN & DUNN, INC.)] | 3 | Current NDC, Legacy NDC, 2 package rows | 20240404_552b0c0e-00f9-498b-8786-ad242703e04b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50804-857-30 | 50804085730 | 1 BOTTLE, PLASTIC in 1 BOX (50804-857-30) / 30 TABLET in 1 BOTTLE, PLASTIC | 2020-02-28 | 2026-06-30 | No | No | Current |