Over-the-counter drug · OTC MONOGRAPH DRUG
Cystex Max Strength UTI Pain Relief NDC 69693-519
Phenazopyridine hydrochloride 99.5 mg/99.5mg · Tablet · Oral · Clarion Brands LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 69693-519-24 | 6969305192469693051924 | 2 BLISTER PACK in 1 CARTON (69693-519-24) / 99.5 mg in 1 BLISTER PACKMarketed from Jul 27, 2026 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Cystex Max Strength UTI Pain Relief
- Generic name (nonproprietary)
- cystex max strength uti pain relief
- Active ingredients
- Phenazopyridine hydrochloride — 99.5 mg/99.5mg
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Clarion Brands LLCNDC labeler code 69693
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 69693-519_57482f71-80d4-b20d-e063-6394a90a0cf4SPL ID 57482f71-80d4-b20d-e063-6394a90a0cf4SPL set ID 57482f71-80d3-b20d-e063-6394a90a0cf4RxCUI 1094147UNII 0EWG668W17UPC 0889476346276
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N469693051924followed by a unit qualifier and the quantityPackage 69693-0519-24. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Use fast relief from urinary pain, burning, urgency and frequency associated with urinary tract infections. Treatment should not exceed 2 days without consulting a doctor; see Directions.
Excerpt only. Read the full label for complete information.
About NDC 69693-519
- What is NDC 69693-519?
- 69693-519 is the product NDC for Cystex Max Strength UTI Pain Relief, Phenazopyridine hydrochloride 99.5 mg/99.5mg tablet, listed with the FDA by Clarion Brands LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Cystex Max Strength UTI Pain Relief.
- What is the active ingredient?
- Phenazopyridine hydrochloride.
- Who is the labeler?
- Clarion Brands LLC, NDC labeler code 69693. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Cystex Max Strength UTI Pain Relief?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Other NDCs under 505G(a)(3)
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
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