Nasal Decongestant
- Product NDC
- 68210-4172
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Phenylephrine Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Spirit Pharmaceuticals LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Substance
- PHENYLEPHRINE HYDROCHLORIDE
- Current FDA listing
- Historical FDA.report record
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 68210-4172-1 | 100 TABLET, COATED in 1 POUCH (68210-4172-1) | 2021-11-22 | No | Current |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|---|
| 51d273c9-804e-4001-844b-ffa15e57265a | Nasal Decongestant | Spirit Pharmaceuticals LLC | 2024-12-13 | HUMAN OTC DRUG LABEL | 5 |