NDC product
GoodSense Eye Drops Original Formula
NDC 50804-141 · Geiss, Destin & Dunn, Inc.
Key facts
| Product NDC | 50804-141 |
|---|---|
| Proprietary name | GoodSense Eye Drops Original Formula |
| Nonproprietary name | tetrahydrozoline HCl |
| Substances | TETRAHYDROZOLINE HYDROCHLORIDE |
| Dosage form | SOLUTION |
| Route | OPHTHALMIC |
| Labeler | Geiss, Destin & Dunn, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M018 |
| Marketing start | Jan 3, 2020 |
| 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: