warnings
Warnings
Uricalm Maximum Strength
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
- Uricalm Maximum Strength
- Generic name
- PHENAZOPYRIDINE HYDOCHLORIDE
- Manufacturer
- Kobayashi Healthcare International, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1d94b45c-ee0b-499d-aca2-e8cd8dd490d2
- SPL ID
- 316e93e7-3627-8e6a-e063-6294a90a1d28
- Version
- 18
- Effective date
- 2025-03-28
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:19:16
| 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 | Uricalm Maximum Strength | openfda.brand_name | |
| generic name | PHENAZOPYRIDINE HYDOCHLORIDE | openfda.generic_name | |
| manufacturer name | Kobayashi Healthcare International, Inc. | openfda.manufacturer_name | |
| ndc | package | 52389-241-02 | openfda.package_ndc |
| ndc | package | 52389-241-36 | openfda.package_ndc |
| ndc | package | 52389-241-04 | openfda.package_ndc |
| ndc | package | 52389-241-12 | openfda.package_ndc |
| ndc | package | 52389-241-48 | openfda.package_ndc |
| ndc | package | 52389-241-24 | openfda.package_ndc |
| ndc | package | 52389-241-03 | openfda.package_ndc |
| ndc | package | 52389-241-28 | openfda.package_ndc |
| ndc | package | 52389-241-01 | openfda.package_ndc |
| ndc | product | 52389-241 | openfda.product_ndc |
| ndc11 | package | 52389024104 | derived:openfda.package_ndc |
| ndc11 | package | 52389024124 | derived:openfda.package_ndc |
| ndc11 | package | 52389024112 | derived:openfda.package_ndc |
| ndc11 | package | 52389024101 | derived:openfda.package_ndc |
| ndc11 | package | 52389024136 | derived:openfda.package_ndc |
| ndc11 | package | 52389024148 | derived:openfda.package_ndc |
| ndc11 | package | 52389024102 | derived:openfda.package_ndc |
| ndc11 | package | 52389024103 | derived:openfda.package_ndc |
| ndc11 | package | 52389024128 | derived:openfda.package_ndc |
| rxcui | 1094149 | openfda.rxcui | |
| rxcui | 1094147 | openfda.rxcui | |
| spl id | 316e93e7-3627-8e6a-e063-6294a90a1d28 | id | |
| spl set id | 1d94b45c-ee0b-499d-aca2-e8cd8dd490d2 | 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.