NDC product
DayTime Sinus
NDC 53345-030 · Humanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd.
Key facts
| Product NDC | 53345-030 |
|---|---|
| Proprietary name | DayTime Sinus |
| Nonproprietary name | acetaminophen, phenylephrine hydrochloride |
| Substances | ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE |
| Dosage form | CAPSULE, LIQUID FILLED |
| Route | ORAL |
| Labeler | Humanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd. |
| 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 | Feb 26, 2015 |
| 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: