MUCUS RELIEF
- Product NDC
- 68210-4158
- 11-digit product format
- 682104158
- Labeler code
- 68210
- Product ID
- 68210-4158_49490f71-0257-e358-e063-6394a90a394a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- GUAIFENESIN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Prodose, Inc.
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-03-10
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- MUCUS RELIEF
- Listing expiration
- 2027-12-31
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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68210-4158-1 | MUCUS RELIEF | 1 in 1 BOTTLE | TABLET | 1 | | 7 |
| 68210-4158-1 | MUCUS RELIEF | 15 in 1 BOTTLE | TABLET | 15 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68210-4158 | MUCUS RELIEF (GUAIFENESIN) TABLET [SPIRIT PHARMACEUTICALS LLC] | 6 | Current NDC, Legacy NDC, 2 package rows | 20241215_7e5de5b0-18f0-4807-8686-da9821f918ce.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68210-4158-1 | 68210415801 | 1 BOTTLE in 1 BOTTLE (68210-4158-1) / 15 TABLET in 1 BOTTLE | 1 bottle | 2021-05-25 | 0000-00-00 | No | No | Current |