Home FDA labels 8cd7c2ff-9e2e-42d3-991f-2dd582a5232d Nephrovesic 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 Nephrovesic
Generic name UVA-URSI, BERBERIS VULGARIS, CHIMAPHILA UMBELLATA, EQUISETUM HYEMALE, HYDRANGEA ARBORESCENS, PETROSELINUM SATIVUM, CANTHARIS, SARSAPARILLA (SMILAX REGELII), OCIMUM SANCTUM, CALCAREA CARBONICA, APIS MELLIFICA, CAUSTICUM, LYCOPODIUM CLAVATUM, MERCURIUS CORROSIVUS, NUX VOMICA, PULSATILLA (PRATENSIS), TEREBINTHINA
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID d7540e9b-aeae-4cab-aa4c-28c1fb6c6625
SPL ID 8cd7c2ff-9e2e-42d3-991f-2dd582a5232d
Version 7
Effective date 2025-04-29
Source export date 2026-09-28
Source partition 7
Source file https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:48:09 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 · 25 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Nephrovesic openfda.brand_name generic name UVA-URSI, BERBERIS VULGARIS, CHIMAPHILA UMBELLATA, EQUISETUM HYEMALE, HYDRANGEA ARBORESCENS, PETROSELINUM SATIVUM, CANTHARIS, SARSAPARILLA (SMILAX REGELII), OCIMUM SANCTUM, CALCAREA CARBONICA, APIS MELLIFICA, CAUSTICUM, LYCOPODIUM CLAVATUM, MERCURIUS CORROSIVUS, NUX VOMICA, PULSATILLA (PRATENSIS), TEREBINTHINA openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-1643-1 openfda.package_ndc ndc product 43742-1643 openfda.product_ndc ndc11 package 43742164301 derived:openfda.package_ndc spl id 8cd7c2ff-9e2e-42d3-991f-2dd582a5232d id spl set id d7540e9b-aeae-4cab-aa4c-28c1fb6c6625 set_id unii SFK828Q2DE openfda.unii unii 269XH13919 openfda.unii unii DD5FO1WKFU openfda.unii unii 2H1576D5WG openfda.unii unii WCK21A9W9J openfda.unii unii 1TH8Q20J0U openfda.unii unii 53GH7MZT1R openfda.unii unii 3Q034RO3BT openfda.unii unii 2E32821G6I openfda.unii unii 3M5V3D1X36 openfda.unii unii 8E272251DI openfda.unii unii 59677RXH25 openfda.unii unii 1WZA4Y92EX openfda.unii unii 34T63W8ULS openfda.unii unii 7S82P3R43Z openfda.unii unii C88X29Y479 openfda.unii unii C5H0QJ6V7F 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: If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.