Home FDA labels 82e09f62-3610-4b7c-aba4-b69b6e25b4eb Bladder Urinary 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 Bladder Urinary
Generic name APIS MELLIFICA, BERBERIS VULGARIS, CANTHARIS, COCCUS CACTI, ECHINACEA (ANGUSTIFOLIA), EQUISETUM HYEMALE, NUX VOMICA, RUBIA TINCTORUM, SARSAPARILLA, STAPHYSAGRIA, THUJA OCCIDENTALIS, ZINGIBER OFFICINALE
Manufacturer Liddell Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 3678b431-789e-453e-b5f4-5cf5b17ac0cc
SPL ID 82e09f62-3610-4b7c-aba4-b69b6e25b4eb
Version 4
Effective date 2024-11-04
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 05:37:12 Harmonized routes table 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.
Harmonized identifiers page 1 of 1 · 20 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Bladder Urinary openfda.brand_name generic name APIS MELLIFICA, BERBERIS VULGARIS, CANTHARIS, COCCUS CACTI, ECHINACEA (ANGUSTIFOLIA), EQUISETUM HYEMALE, NUX VOMICA, RUBIA TINCTORUM, SARSAPARILLA, STAPHYSAGRIA, THUJA OCCIDENTALIS, ZINGIBER OFFICINALE openfda.generic_name manufacturer name Liddell Laboratories, Inc. openfda.manufacturer_name ndc package 50845-0244-1 openfda.package_ndc ndc product 50845-0244 openfda.product_ndc ndc11 package 50845024401 derived:openfda.package_ndc spl id 82e09f62-3610-4b7c-aba4-b69b6e25b4eb id spl set id 3678b431-789e-453e-b5f4-5cf5b17ac0cc set_id unii 269XH13919 openfda.unii unii 00543AP1JV openfda.unii unii LZB7TFX1LT openfda.unii unii 2H1576D5WG openfda.unii unii 1TH8Q20J0U openfda.unii unii 3Q034RO3BT openfda.unii unii 0T0DQN8786 openfda.unii unii VB06AV5US8 openfda.unii unii 0SVP95L23G openfda.unii unii 59677RXH25 openfda.unii unii 7S82P3R43Z openfda.unii unii C5529G5JPQ openfda.unii
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: Do not use if you have ever has an allergic reaction to this product or any of its ingredients. Stop use and ask a doctor if symptoms persist for more than 3 days, are severe, or you experience fever, chills, back pain or bloody urine. You may have a serious condition that requires professional treatment. Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use. Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.