warnings
Warning Do not exceed recommended dosage
Quality Choice Urinary Pain 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
- Brand name
- Quality Choice Urinary Pain Relief
- Generic name
- PHENAZOPYRIDINE HYDROCHLORIDE
- Manufacturer
- Chain Drug Marketing Association
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 45e0cc2f-4a25-40ef-86ed-d1212815d751
- SPL ID
- 79ec9cb2-5205-4e0a-9a82-35c5cdc77a74
- Version
- 1
- Effective date
- 2025-12-02
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:38:44
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | Quality Choice Urinary Pain Relief | openfda.brand_name | |
| generic name | PHENAZOPYRIDINE HYDROCHLORIDE | openfda.generic_name | |
| manufacturer name | Chain Drug Marketing Association | openfda.manufacturer_name | |
| ndc | package | 83324-201-30 | openfda.package_ndc |
| ndc | product | 83324-201 | openfda.product_ndc |
| ndc11 | package | 83324020130 | derived:openfda.package_ndc |
| rxcui | 1094126 | openfda.rxcui | |
| spl id | 79ec9cb2-5205-4e0a-9a82-35c5cdc77a74 | id | |
| spl set id | 45e0cc2f-4a25-40ef-86ed-d1212815d751 | set_id | |
| unii | 0EWG668W17 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.