Home FDA labels 58ca2513-a466-52d6-e063-6394a90a634c Renapath 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 Renapath
Generic name BENZOICUM ACIDUM, BERBERIS VULGARIS, BRYONIA, DNA, EUPATORIUM PURPUREUM, GLANDULA SUPRARENALIS SUIS, HYDRANGEA ARBORESCENS, HYPOTHALAMUS, MERCURIUS CORROSIVUS, PANCREAS SUIS, PAREIRA BRAVA, PETROSELINUM SATIVUM, PITUITARUM POSTERIUM, RUBIA TINCTORUM, SARSAPARILLA, SOLIDAGO VIRGAUREA, THYROIDINUM (BOVINE), UVA-URSI
Manufacturer Energetix Corporation
Product type HUMAN OTC DRUG
SPL set ID 1a37b994-9470-4266-a4e1-008538ea0edf
SPL ID 58ca2513-a466-52d6-e063-6394a90a634c
Version 13
Effective date 2026-08-11
Source export date 2026-09-28
Source partition 2
Source file https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:15:27 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 · 26 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Renapath openfda.brand_name generic name BENZOICUM ACIDUM, BERBERIS VULGARIS, BRYONIA, DNA, EUPATORIUM PURPUREUM, GLANDULA SUPRARENALIS SUIS, HYDRANGEA ARBORESCENS, HYPOTHALAMUS, MERCURIUS CORROSIVUS, PANCREAS SUIS, PAREIRA BRAVA, PETROSELINUM SATIVUM, PITUITARUM POSTERIUM, RUBIA TINCTORUM, SARSAPARILLA, SOLIDAGO VIRGAUREA, THYROIDINUM (BOVINE), UVA-URSI openfda.generic_name manufacturer name Energetix Corporation openfda.manufacturer_name ndc package 64578-0103-1 openfda.package_ndc ndc product 64578-0103 openfda.product_ndc ndc11 package 64578010301 derived:openfda.package_ndc spl id 58ca2513-a466-52d6-e063-6394a90a634c id spl set id 1a37b994-9470-4266-a4e1-008538ea0edf set_id unii SFK828Q2DE openfda.unii unii 395A3P448Z openfda.unii unii 51FI676N6F openfda.unii unii 2H1576D5WG openfda.unii unii 8SKN0B0MIM openfda.unii unii 1TH8Q20J0U openfda.unii unii 53GH7MZT1R openfda.unii unii MN18OTN73W openfda.unii unii L0PFEMQ1DT openfda.unii unii 0SVP95L23G openfda.unii unii 3M5V3D1X36 openfda.unii unii S6G2NLH4Y7 openfda.unii unii T7J046YI2B openfda.unii unii 398IYQ16YV openfda.unii unii 1WZA4Y92EX openfda.unii unii 0VYG5PVN5Q openfda.unii unii 5405K23S50 openfda.unii unii 9Y3J3362RY 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 health 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.