What is NDC 73436-1221?

73436-1221 is the product NDC for Uti Infection Control, Methenamine 162 mg/1; Sodium salicylate 162.5 mg/1 tablet, listed with the FDA by CADENCE HEALTH, INC.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Uti Infection Control (Methenamine, Sodium Salicylate).

What is the active ingredient?

Methenamine, Sodium salicylate.

CADENCE HEALTH, INC., NDC labeler code 73436. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Uti Infection Control?

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.

Uti Infection Control NDC 73436-1221

NDC codes

FDA NDC Directory

Product NDC (as listed)73436-1221Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73436-1221Add 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
73436-1221-2	7343612210273436122102	1 BLISTER PACK in 1 CARTON (73436-1221-2) / 12 TABLET in 1 BLISTER PACKMarketed from Apr 15, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Uti Infection Control
Generic name (nonproprietary): methenamine, sodium salicylate
Active ingredients: Methenamine — 162 mg/1Sodium salicylate — 162.5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: CADENCE HEALTH, INC.NDC labeler code 73436
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Apr 6, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 73436-1221_4ece7cbb-cba6-f159-e063-6294a90a99fcSPL ID 4ece7cbb-cba6-f159-e063-6294a90a99fcSPL set ID 4d249fbc-98cf-44e4-b347-1c056dcf3cf3RxCUI 1489932UNII J50OIX95QV, WIQ1H85SYP

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

N473436122102 followed by a unit qualifier and the quantity

Package 73436-1221-02. 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 Apr 6, 2026.

Indications (excerpt from the label)

Uses Temporarily relieves: pain and 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 73436-1221

What is NDC 73436-1221?: 73436-1221 is the product NDC for Uti Infection Control, Methenamine 162 mg/1; Sodium salicylate 162.5 mg/1 tablet, listed with the FDA by CADENCE HEALTH, INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Uti Infection Control (Methenamine, Sodium Salicylate).
What is the active ingredient?: Methenamine, Sodium salicylate.
Who is the labeler?: CADENCE HEALTH, INC., NDC labeler code 73436. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Uti Infection Control?: 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.

Uti Infection Control (Methenamine, sodium salicylate) NDC 73436-1221