What is NDC 72090-065?

72090-065 is the product NDC for Gencare-Urinary Tract Defense, Methenamine 162 mg/1; Sodium salicylate 162.5 mg/1 tablet, listed with the FDA by PIONEER LIFE SCIENCES, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Gencare-Urinary Tract Defense (Methenamine, sodium salicylate).

What is the active ingredient?

Methenamine, Sodium salicylate.

PIONEER LIFE SCIENCES, LLC, NDC labeler code 72090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Gencare-Urinary Tract Defense?

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.

Gencare-Urinary Tract Defense NDC 72090-065

NDC codes

FDA NDC Directory

Product NDC (as listed)72090-065Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72090-0065Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
72090-065-01	7209000650172090006501	2 BLISTER PACK in 1 CARTON (72090-065-01) / 24 TABLET in 1 BLISTER PACKMarketed from Aug 10, 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): Gencare-Urinary Tract Defense
Generic name (nonproprietary): methenamine, sodium salicylate
Active ingredients: Methenamine — 162 mg/1Sodium salicylate — 162.5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: PIONEER LIFE SCIENCES, LLCNDC labeler code 72090
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Aug 10, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 72090-065_7de585a8-37d4-4221-aa91-da8dfc597ee9SPL ID 7de585a8-37d4-4221-aa91-da8dfc597ee9SPL set ID 42e443d9-83f8-4868-8c1b-34fe4dc0ed8cRxCUI 1489932UNII J50OIX95QV, WIQ1H85SYPUPC 0372090005044

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

N472090006501 followed by a unit qualifier and the quantity

Package 72090-0065-01. 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 Aug 10, 2026.

Indications (excerpt from the label)

Uses Temporarily relieves: ■Pain & burning ■ frequency and urgency of urination

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72090-065

What is NDC 72090-065?: 72090-065 is the product NDC for Gencare-Urinary Tract Defense, Methenamine 162 mg/1; Sodium salicylate 162.5 mg/1 tablet, listed with the FDA by PIONEER LIFE SCIENCES, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Gencare-Urinary Tract Defense (Methenamine, sodium salicylate).
What is the active ingredient?: Methenamine, Sodium salicylate.
Who is the labeler?: PIONEER LIFE SCIENCES, LLC, NDC labeler code 72090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Gencare-Urinary Tract Defense?: 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.

Gencare-Urinary Tract Defense (Methenamine, sodium salicylate) NDC 72090-065