UTI EMERGENCY RELIEF

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: UTI EMERGENCY RELIEF
Generic name: METHENAMINE, SODIUM SALICYLATE, AND PHENAZOPYRIDINE HYDROCHLORIDE KIT
Manufacturer: CADENCE HEALTH, INC.
Product type: HUMAN OTC DRUG
SPL set ID: 3a923df5-15ed-404d-8741-33a9793cb7f5
SPL ID: 4ece6e64-c81e-0fa8-e063-6294a90ac6d1
Version: 2
Effective date: 2026-04-06
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:27:25

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		UTI EMERGENCY RELIEF	openfda.brand_name
generic name		METHENAMINE, SODIUM SALICYLATE, AND PHENAZOPYRIDINE HYDROCHLORIDE KIT	openfda.generic_name
manufacturer name		CADENCE HEALTH, INC.	openfda.manufacturer_name
ndc	package	73436-1221-2	openfda.package_ndc
ndc	package	73436-2441-2	openfda.package_ndc
ndc	package	73436-4882-4	openfda.package_ndc
ndc	product	73436-4882	openfda.product_ndc
ndc11	package	73436122102	derived:openfda.package_ndc
ndc11	package	73436244102	derived:openfda.package_ndc
ndc11	package	73436488204	derived:openfda.package_ndc
rxcui		1489932	openfda.rxcui
rxcui		1094147	openfda.rxcui
spl id		4ece6e64-c81e-0fa8-e063-6294a90ac6d1	id
spl set id		3a923df5-15ed-404d-8741-33a9793cb7f5	set_id

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Reye's Syndrome (UTI Infection Control Only) Reye’s syndrome: Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye’s syndrome, a rare but serious illness. Stomach bleeding warning: This product contains a non-steroidal anti-inflammatory drug (NSAID), which may cause stomach bleeding. The chance is higher if you: are 60 or older have stomach ulcers or bleeding problems take a blood thinning (anticoagulant) or steroid drug take other drugs containing an NSAID (aspirin, ibuprofen, naproxen, or others) have 3 or more alcoholic drinks every day while using this product take more or for a longer time than directed Do Not Exceed (UTI Pain Relief Only) Do not exceed recommended dosage

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.