Mucus Relief
- Product NDC
- 17714-152
- 11-digit product format
- 177140152
- Labeler code
- 17714
- Product ID
- 17714-152_5cc992c7-a1b3-46be-e053-2991aa0a1f8f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin 400 mg
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Advance Pharmaceutical Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-11-01
- Substance
- GUAIFENESIN
- Active strength
- 400 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- 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 Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17714-152-01 | Mucus Relief | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17714-152 | MUCUS RELIEF (GUAIFENESIN 400 MG) TABLET [ADVANCE PHARMACEUTICAL INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20171031_5b78bbe9-806c-443f-bc23-351e5342355f.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 |
|---|
| 17714-152-01 | 17714015201 | 100 TABLET in 1 BOTTLE (17714-152-01) | 100 tablet | 2016-11-01 | 0000-00-00 | No | No | Current |