Home FDA labels 0e76e858-e00d-c0d8-e063-6394a90a946b D05 KDNY-DRN 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 D05 KDNY-DRN
Generic name APIS MELLIFERA, ASPARAGUS, BERBERIS VULGARIS ROOT BARK, LYTTA VESICATORIA, CHELIDONIUM MAJUS, JUNIPER BERRY, MAGNESIUM CHLORIDE, SODIUM CHLORIDE, POPULUS TREMULOIDES BARK, RHUS AROMATICA ROOT BARK, RUBIA TINCTORUM ROOT, SAW PALMETTO, SOLIDAGO VIRGAUREA FLOWERING TOP, TARAXACUM OFFICINALE, AND ARCTOSTAPHYLOS UVA-URSI LEAF
Manufacturer Apex Energetics Inc.
Product type HUMAN OTC DRUG
SPL set ID 146800dc-bb1a-4d4c-803a-156a9fba600d
SPL ID 0e76e858-e00d-c0d8-e063-6394a90a946b
Version 4
Effective date 2024-01-08
Source export date 2026-09-28
Source partition 8
Source file https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:56:00 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name D05 KDNY-DRN openfda.brand_name generic name APIS MELLIFERA, ASPARAGUS, BERBERIS VULGARIS ROOT BARK, LYTTA VESICATORIA, CHELIDONIUM MAJUS, JUNIPER BERRY, MAGNESIUM CHLORIDE, SODIUM CHLORIDE, POPULUS TREMULOIDES BARK, RHUS AROMATICA ROOT BARK, RUBIA TINCTORUM ROOT, SAW PALMETTO, SOLIDAGO VIRGAUREA FLOWERING TOP, TARAXACUM OFFICINALE, AND ARCTOSTAPHYLOS UVA-URSI LEAF openfda.generic_name manufacturer name Apex Energetics Inc. openfda.manufacturer_name ndc package 63479-0405-1 openfda.package_ndc ndc product 63479-0405 openfda.product_ndc ndc11 package 63479040501 derived:openfda.package_ndc spl id 0e76e858-e00d-c0d8-e063-6394a90a946b id spl set id 146800dc-bb1a-4d4c-803a-156a9fba600d set_id unii 02F3473H9O openfda.unii unii 7E889U5RNN openfda.unii unii J7WWH9M8QS openfda.unii unii Z1EJP3037Z openfda.unii unii 1TH8Q20J0U openfda.unii unii 39981FM375 openfda.unii unii 3Q034RO3BT openfda.unii unii 451W47IQ8X openfda.unii unii 0SVP95L23G openfda.unii unii 3M5V3D1X36 openfda.unii unii 5543O0CEID openfda.unii unii Q3H36W0J42 openfda.unii unii O84B5194RL openfda.unii unii 7S82P3R43Z openfda.unii unii 5405K23S50 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, backache, fatigue, swelling, 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.