NDC product
Cystex Max Strength UTI Pain Relief
NDC 69693-519 · Clarion Brands LLC
Key facts
| Product NDC | 69693-519 |
|---|---|
| Proprietary name | Cystex Max Strength UTI Pain Relief |
| Nonproprietary name | Cystex Max Strength UTI Pain Relief |
| Substances | PHENAZOPYRIDINE HYDROCHLORIDE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Clarion Brands LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | 505G(a)(3) |
| Marketing start | Jul 27, 2026 |
| Listing certified through | Dec 31, 2027 |
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: