MUCUS RELIEF
- Product NDC
- 57896-794
- 11-digit product format
- 578960794
- Labeler code
- 57896
- Product ID
- 57896-794_284e3828-f883-997b-e063-6394a90ac514
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Geri-Care Pharmaceuticals, Corp
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2004-01-01
- 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
- 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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 57896-794-01 | MUCUS RELIEF | 100 in 1 BOTTLE | TABLET | 100 | | 7 |
| 57896-794-03 | MUCUS RELIEF | 30 in 1 BOTTLE | TABLET | 30 | | 7 |
| 57896-794-06 | MUCUS RELIEF | 60 in 1 BOTTLE | TABLET | 60 | | 7 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| GUAIFENESIN | ACTIVE INGREDIENT | 495W7451VQ | MUCUS RELIEF (GUAIFENESIN) TABLET [GERI-CARE PHARMACEUTICALS, CORP] | 1 | |
| GUAIFENESIN | ACTIVE MOIETY | 495W7451VQ | MUCUS RELIEF (GUAIFENESIN) TABLET [GERI-CARE PHARMACEUTICALS, CORP] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | MUCUS RELIEF (GUAIFENESIN) TABLET [GERI-CARE PHARMACEUTICALS, CORP] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | MUCUS RELIEF (GUAIFENESIN) TABLET [GERI-CARE PHARMACEUTICALS, CORP] | 1 | |
| MALTODEXTRIN | INACTIVE INGREDIENT | 7CVR7L4A2D | MUCUS RELIEF (GUAIFENESIN) TABLET [GERI-CARE PHARMACEUTICALS, CORP] | 1 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | MUCUS RELIEF (GUAIFENESIN) TABLET [GERI-CARE PHARMACEUTICALS, CORP] | 1 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | MUCUS RELIEF (GUAIFENESIN) TABLET [GERI-CARE PHARMACEUTICALS, CORP] | 1 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | MUCUS RELIEF (GUAIFENESIN) TABLET [GERI-CARE PHARMACEUTICALS, CORP] | 1 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | MUCUS RELIEF (GUAIFENESIN) TABLET [GERI-CARE PHARMACEUTICALS, CORP] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 57896-794 | MUCUS RELIEF (GUAIFENESIN) TABLET [GERI-CARE PHARMACEUTICALS, CORP] | 7 | Current NDC, Legacy NDC, 3 package rows | 20241204_bb72de5d-d3c0-42fc-ae52-a3ad95214af5.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 |
|---|
| 57896-794-01 | 57896079401 | 100 TABLET in 1 BOTTLE (57896-794-01) | 100 tablet | 2012-01-01 | 0000-00-00 | No | No | Current |
| 57896-794-03 | 57896079403 | 30 TABLET in 1 BOTTLE (57896-794-03) | 30 tablet | 2012-01-01 | 0000-00-00 | No | No | Current |
| 57896-794-06 | 57896079406 | 60 TABLET in 1 BOTTLE (57896-794-06) | 60 tablet | 2018-09-01 | 0000-00-00 | No | No | Current |