NDC product
Sinus Pressure plus Pain PE
NDC 36800-320 · TOPCO ASSOCIATES LLC
Key facts
| Product NDC | 36800-320 |
|---|---|
| Proprietary name | Sinus Pressure plus Pain PE |
| Nonproprietary name | ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE |
| Substances | ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE |
| Dosage form | TABLET, COATED |
| Route | ORAL |
| Labeler | TOPCO ASSOCIATES LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Pharmacologic classes | Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
| Marketing start | Jun 18, 2021 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: