Mucus Relief
- Product NDC
- 37808-935
- 11-digit product format
- 378080935
- Labeler code
- 37808
- Product ID
- 37808-935_884b612b-7aff-4e32-aa00-a77e28346a7f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- H E B
- Application
- ANDA207342
- Marketing category
- ANDA
- Marketing start
- 2021-05-28
- 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 37808-935-40 | 37808093540 | 1 BOTTLE, PLASTIC in 1 BOX (37808-935-40) / 40 TABLET in 1 BOTTLE, PLASTIC | 2021-05-28 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Drug Facts | H E B | 2022-11-07 | HUMAN OTC DRUG LABEL | 2 |