Mucus Relief
- Product NDC
- 54738-980
- 11-digit product format
- 547380980
- Labeler code
- 54738
- Product ID
- 54738-980_73570295-8ab7-1c19-e053-2991aa0a6b82
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin 200 mg
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Richmond Pharmaceuticals, Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-03-01
- Substance
- GUAIFENESIN
- Active strength
- 200 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 | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 495W7451VQ |
| Rxcui | 197741 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 54738-980-01 | Mucus Relief | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 54738-980 | MUCUS RELIEF (GUAIFENESIN 200 MG) TABLET [RICHMOND PHARMACEUTICALS, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20180822_e20927a1-d402-48c1-ba00-0745ddd0a0e7.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 |
|---|
| 54738-980-01 | 54738098001 | 100 TABLET in 1 BOTTLE (54738-980-01) | 100 tablet | 2016-03-01 | 0000-00-00 | No | No | Current |