MUCUS RELIEF
- Product NDC
- 37835-412
- 11-digit product format
- 378350412
- Labeler code
- 37835
- Product ID
- 37835-412_33d4125b-83ad-18f0-e063-6394a90a679d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- GUAIFENESIN
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bi-Mart
- Application
- ANDA213420
- Marketing category
- ANDA
- Marketing start
- 2020-12-18
- Substance
- GUAIFENESIN
- Active strength
- 1200 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 | 1200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 495W7451VQ |
| Rxcui | 310621 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 37835-412-28 | MUCUS RELIEF | 28 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 28 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37835-412 | MUCUS RELIEF (GUAIFENESIN) TABLET, EXTENDED RELEASE [BI-MART] | 1 | Current NDC, 1 package rows | 20250501_d995a6a5-d68b-44e4-9281-32c5417fb5e3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 37835-412-28 | 37835041228 | 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (37835-412-28) | 2025-04-01 | No | No | Current |