Mucus Relief
- Product NDC
- 0904-6986
- 11-digit product format
- 009046986
- Labeler code
- 0904
- Product ID
- 0904-6986_8bd5552a-8889-4aba-a40b-b4b0bcf99503
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA209215
- Marketing category
- ANDA
- Marketing start
- 2019-09-23
- Substance
- GUAIFENESIN
- Active strength
- 600 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 | 600 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 495W7451VQ |
| Rxcui | 636522 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0904-6986-40 | Mucus Relief | 500 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 500 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-6986 | MUCUS RELIEF (GUAIFENESIN) TABLET, EXTENDED RELEASE [MAJOR PHARMACEUTICALS] | 4 | Current NDC, Legacy NDC, 1 package rows | 20220106_4d98920b-caf7-42d9-bd08-859d27b6d76a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-6986-40 | 00904698640 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (0904-6986-40) | 2019-09-23 | 0000-00-00 | No | No | Current |