Quality Choice Mucus Relief
- Product NDC
- 83324-194
- 11-digit product format
- 833240194
- Labeler code
- 83324
- Product ID
- 83324-194_87c7f7bf-b860-4ba5-9574-e9f0d9802b09
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Chain Drug Marketing Association
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-12-02
- 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
- Quality Choice Mucus Relief
- 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 Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 83324-194-50 | Quality Choice Mucus Relief | 50 in 1 BOTTLE | TABLET | 50 | | 1 |
| 83324-194-50 | Quality Choice Mucus Relief | 1 in 1 CARTON | TABLET | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83324-194-50 | 83324019450 | 1 BOTTLE in 1 CARTON (83324-194-50) / 50 TABLET in 1 BOTTLE | 1 bottle | 2025-12-02 | No | No | Current |