Home FDA labels 0e764c29-02d9-6485-e063-6394a90a6a45 A12 DTX-KIDNEY 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 A12 DTX-KIDNEY
Generic name APIS MELLIFICA, BERBERIS VULGARIS, BETULA PUBESCENS BARK, BETULA VERRUCOSA LEAF, BOS TAURUS KIDNEY, BOS TAURUS URINARY BLADDER, CITRICUM ACIDUM, CITRUS LIMONUM, FAGUS SYLVESTRIS FLOWER BUD, NATRUM MURIATICUM, PETROSELINUM SATIVUM, QUERCUS ROBUR FLOWER BUD, SINUSITISINUM, SOLIDAGO VIRGAUREA
Manufacturer Apex Energetics Inc.
Product type HUMAN OTC DRUG
SPL set ID bf52e26f-aa27-87ca-e053-2995a90a23e7
SPL ID 0e764c29-02d9-6485-e063-6394a90a6a45
Version 2
Effective date 2024-01-08
Source export date 2026-10-12
Source partition 14
Source file https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 03:12:48 Harmonized routes table Harmonized routes SUBLINGUAL
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 · 22 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name A12 DTX-KIDNEY openfda.brand_name generic name APIS MELLIFICA, BERBERIS VULGARIS, BETULA PUBESCENS BARK, BETULA VERRUCOSA LEAF, BOS TAURUS KIDNEY, BOS TAURUS URINARY BLADDER, CITRICUM ACIDUM, CITRUS LIMONUM, FAGUS SYLVESTRIS FLOWER BUD, NATRUM MURIATICUM, PETROSELINUM SATIVUM, QUERCUS ROBUR FLOWER BUD, SINUSITISINUM, SOLIDAGO VIRGAUREA openfda.generic_name manufacturer name Apex Energetics Inc. openfda.manufacturer_name ndc package 63479-0112-1 openfda.package_ndc ndc product 63479-0112 openfda.product_ndc ndc11 package 63479011201 derived:openfda.package_ndc spl id 0e764c29-02d9-6485-e063-6394a90a6a45 id spl set id bf52e26f-aa27-87ca-e053-2995a90a23e7 set_id unii 5HOC10FSIC openfda.unii unii 1TH8Q20J0U openfda.unii unii AGN709ANTJ openfda.unii unii 5HW39H9KDH openfda.unii unii 451W47IQ8X openfda.unii unii 0SLJ2C1IHA openfda.unii unii 3R504894L9 openfda.unii unii B575563DM5 openfda.unii unii 1WZA4Y92EX openfda.unii unii XF417D3PSL openfda.unii unii 7S82P3R43Z openfda.unii unii 5405K23S50 openfda.unii unii 6D5V13045W openfda.unii unii VC5I578BE3 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. Do not use if clear seal over the cap is broken or missing. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if urinary discomfort, headache, vertigo, water retention, backache, or other symptoms do not improve within 7 days or are accompanied by fever.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.