Home FDA labels 58c9102c-b68a-6394-e063-6394a90a9a3a Kidney-Tone 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 Kidney-Tone
Generic name AGRIMONIA EUPATORIA, BERBERIS VULGARIS, CALCAREA OXALICA, CALCAREA PHOSPHORICA, CANTHARIS, ECHINACEA, EQUISETUM ARVENSE, FERRUM PHOSPHORICUM, LYCOPODIUM CLAVATUM, PAREIRA BRAVA, PETROSELINUM SATIVUM, RUBIA TINCTORUM, SARSAPARILLA, SOLIDAGO VIRGAUREA, UVA-URSI.
Manufacturer Energetix Corporation
Product type HUMAN OTC DRUG
SPL set ID 9ca2cbee-5251-4e96-b48b-823bc5605c2c
SPL ID 58c9102c-b68a-6394-e063-6394a90a9a3a
Version 10
Effective date 2026-08-11
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 05:26:45 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Kidney-Tone openfda.brand_name generic name AGRIMONIA EUPATORIA, BERBERIS VULGARIS, CALCAREA OXALICA, CALCAREA PHOSPHORICA, CANTHARIS, ECHINACEA, EQUISETUM ARVENSE, FERRUM PHOSPHORICUM, LYCOPODIUM CLAVATUM, PAREIRA BRAVA, PETROSELINUM SATIVUM, RUBIA TINCTORUM, SARSAPARILLA, SOLIDAGO VIRGAUREA, UVA-URSI. openfda.generic_name manufacturer name Energetix Corporation openfda.manufacturer_name ndc package 64578-0149-1 openfda.package_ndc ndc product 64578-0149 openfda.product_ndc ndc11 package 64578014901 derived:openfda.package_ndc spl id 58c9102c-b68a-6394-e063-6394a90a9a3a id spl set id 9ca2cbee-5251-4e96-b48b-823bc5605c2c set_id unii 395A3P448Z openfda.unii unii 2H1576D5WG openfda.unii unii 1TH8Q20J0U openfda.unii unii 91D9GV0Z28 openfda.unii unii 4PP86KK527 openfda.unii unii 3Q034RO3BT openfda.unii unii 91GQH8I5F7 openfda.unii unii EBU0U94820 openfda.unii unii 4N9P6CC1DX openfda.unii unii 0SVP95L23G openfda.unii unii 3M5V3D1X36 openfda.unii unii 1WZA4Y92EX openfda.unii unii 5405K23S50 openfda.unii unii C88X29Y479 openfda.unii unii 1DP6Y6B65Z 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 In case of overdose, get medical help or contact a Poison Control Center right away. If pregnant or breast - feeding , ask a healthcare professional before use. Keep out of reach of children.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.