FDA label 413a3983-6a9f-eecb-e063-6294a90a8d75

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)

SPL set ID: 6a39f966-0e15-4f46-e053-2991aa0a00a0
SPL ID: 413a3983-6a9f-eecb-e063-6294a90a8d75
Version: 4
Effective date: 2025-10-15
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:25:19

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 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		413a3983-6a9f-eecb-e063-6294a90a8d75	id
spl set id		6a39f966-0e15-4f46-e053-2991aa0a00a0	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 Frequent urination can also be caused by: • Urinary tract infections (UTI).  • diabetes.  • early pregnancy.  • other more serious conditions. If you think you might have one of these conditions, it is important to see your doctor before use. As with any drug, ask a doctor before use if pregnant or breast-feeding. Do not use:  • more than directed.  • if you have a known allergy to any ingredient in this product. Consult a physician if symptoms persist for more than 7 days or worsen. Keep this and all medications out of reach of children. In case of accidental overdose, contact a medical professional or Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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