What is NDC 73436-4882?

73436-4882 is the product NDC for Uti Emergency Relief kit, 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 Emergency Relief (Methenamine, sodium salicylate, and phenazopyridine hydrochloride kit).

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 Emergency 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.

Uti Emergency Relief NDC 73436-4882

NDC codes

FDA NDC Directory

Product NDC (as listed)73436-4882Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73436-4882Add 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
73436-4882-4	7343648820473436488204	1 KIT in 1 CARTON (73436-4882-4) * 1 BLISTER PACK in 1 CARTON (73436-1221-2) / 12 TABLET in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON (73436-2441-2) / 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 Emergency Relief
Generic name (nonproprietary): methenamine, sodium salicylate, and phenazopyridine hydrochloride kit
Dosage form: Kit
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 73436-4882_4ece6e64-c81e-0fa8-e063-6294a90ac6d1SPL ID 4ece6e64-c81e-0fa8-e063-6294a90ac6d1SPL set ID 3a923df5-15ed-404d-8741-33a9793cb7f5RxCUI 1094147, 1489932

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N473436488204 followed by a unit qualifier and the quantity

Package 73436-4882-04. 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 UTI Infection Control Temporarily relieves: pain and burning frequency and urgency of urination UTI Pain Relief Fast relief from urinary pain, burning, urgency and frequency associated with urinary tract infections. Treatment should not exceed 2 days; see Directions.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 73436-4882

What is NDC 73436-4882?: 73436-4882 is the product NDC for Uti Emergency Relief kit, 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 Emergency Relief (Methenamine, sodium salicylate, and phenazopyridine hydrochloride kit).
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 Emergency 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.