Mucus Relief
- Product NDC
- 82725-1012
- 11-digit product format
- 827251012
- Labeler code
- 82725
- Product ID
- 82725-1012_395687f6-95e4-578c-e063-6394a90a1e6a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin 400 mg
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cabinet Health, Inc.
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-11-01
- 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 |
|---|
| 82725-1012-1 | Mucus Relief | 200 in 1 BOTTLE | TABLET | 200 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82725-1012 | MUCUS RELIEF (GUAIFENESIN 400 MG) TABLET [CABINET HEALTH, INC.] | 1 | Current NDC, 1 package rows | 20241114_26a51b0e-039c-663c-e063-6394a90ad384.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82725-1012-1 | 82725101201 | 200 TABLET in 1 BOTTLE (82725-1012-1) | 200 tablet | 2024-11-01 | No | No | Current |