Mucus Relief
- Product NDC
- 67091-404
- 11-digit product format
- 670910404
- Labeler code
- 67091
- Product ID
- 67091-404_f9159d83-e679-0576-e053-6394a90a651a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- WINCO FOODS, LLC
- Application
- ANDA213420
- Marketing category
- ANDA
- Marketing start
- 2023-04-11
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 495W7451VQ | GUAIFENESIN | 93-14-1 | GUAIFENESIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67091-404-02 | 67091040402 | 2 BLISTER PACK in 1 CARTON (67091-404-02) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 2 blister pack | 2023-04-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| 1204A-WNC-2023-0411 | WINCO FOODS, LLC | 2023-04-11 | HUMAN OTC DRUG LABEL | 2 |