MUCUS RELIEF
- Product NDC
- 41226-272
- 11-digit product format
- 412260272
- Labeler code
- 41226
- Product ID
- 41226-272_88f1545a-6dbd-54f8-e053-2995a90a4138
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- KROGER COMPANY
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-06-03
- 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 |
|---|
| 41226-272-03 | MUCUS RELIEF | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41226-272 | MUCUS RELIEF (GUAIFENESIN) TABLET [KROGER COMPANY] | 2 | Current NDC, Legacy NDC, 1 package rows | 20190603_813b1db2-a177-77c6-e053-2a91aa0ac73b.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 |
|---|
| 41226-272-03 | 41226027203 | 30 TABLET in 1 BOTTLE (41226-272-03) | 30 tablet | 2019-06-03 | 0000-00-00 | No | No | Current |