Mucus Relief
- Product NDC
- 70677-1052
- 11-digit product format
- 706771052
- Labeler code
- 70677
- Product ID
- 70677-1052_cd45b857-7fb8-4b56-903d-149659d6cd15
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA207342
- Marketing category
- ANDA
- Marketing start
- 2023-03-31
- 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
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 |
|---|
| 70677-1052-1 | 70677105201 | 20 BLISTER PACK in 1 CARTON (70677-1052-1) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 20 blister pack | 2023-03-31 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Drug Facts | Strategic Sourcing Services LLC | 2023-04-21 | HUMAN OTC DRUG LABEL | 1 |