Mucus Relief
- Product NDC
- 37808-935
- 11-digit product format
- 378080935
- Labeler code
- 37808
- Product ID
- 37808-935_884b612b-7aff-4e32-aa00-a77e28346a7f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- H E B
- Application
- ANDA207342
- Marketing category
- ANDA
- Marketing start
- 2021-05-28
- 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 |
|---|
| 37808-935-40 | Mucus Relief | 40 in 1 BOTTLE, PLASTIC | TABLET | 40 | | 2 |
| 37808-935-40 | Mucus Relief | 1 in 1 BOX | TABLET | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-935 | MUCUS RELIEF (GUAIFENESIN) TABLET [H E B] | 2 | Current NDC, Legacy NDC, 2 package rows | 20221108_562b6ab6-4795-4909-8008-e919173844c9.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 |
|---|
| 37808-935-40 | 37808093540 | 1 BOTTLE, PLASTIC in 1 BOX (37808-935-40) / 40 TABLET in 1 BOTTLE, PLASTIC | 2021-05-28 | 0000-00-00 | No | No | Current |