Mucus Relief
- Product NDC
- 37808-830
- 11-digit product format
- 378080830
- Labeler code
- 37808
- Product ID
- 37808-830_b74e7c92-7fe7-4455-9af9-6ebe568639b7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- H E B
- Application
- ANDA207342
- Marketing category
- ANDA
- Marketing start
- 2023-06-05
- 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 Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 37808-830-20 | Mucus Relief | 1 in 1 BOX | TABLET, EXTENDED RELEASE | 1 | | 4 |
| 37808-830-20 | Mucus Relief | 20 in 1 BOTTLE, PLASTIC | TABLET, EXTENDED RELEASE | 20 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-830 | MUCUS RELIEF (GUAIFENESIN) TABLET, EXTENDED RELEASE [H E B] | 4 | Current NDC, 2 package rows | 20250321_efebda97-5234-451c-a854-91a32303a6b7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 37808-830-20 | 37808083020 | 1 BOTTLE, PLASTIC in 1 BOX (37808-830-20) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC | 2023-06-05 | No | No | Current |