MUCUS RELIEF
- Product NDC
- 57896-614
- 11-digit product format
- 578960614
- Labeler code
- 57896
- Product ID
- 57896-614_ee13ae41-86e0-12f7-e053-2a95a90a2a13
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Geri-Care Pharmaceuticals, Corp
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-09-01
- Marketing end
- 2023-11-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 57896-614-01 | 57896061401 | 100 TABLET in 1 BOTTLE (57896-614-01) | 100 tablet | 2021-09-01 | 0000-00-00 | No | No | Current |
| 57896-614-06 | 57896061406 | 60 TABLET in 1 BOTTLE (57896-614-06) | 60 tablet | 2021-09-01 | 0000-00-00 | No | No | Current |