Home FDA labels 0e767659-f964-7c88-e063-6294a90a0f64 A13 DTX-LIVER 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 A13 DTX-LIVER
Generic name BOS TAURUS GALLBLADDER, BRYONIA, CHELIDONIUM MAJUS, CHOLESTERINUM, HEPAR SULPHURIS CALCAREUM , JUNIPERUS COMMUNIS STEM, LYCOPODIUM CLAVATUM, NATRUM SULPHURICUM, PHOSPHORUS, RHAMNUS PURSHIANA, ROSMARINUS OFFICINALIS, SECALE CEREALE WHOLE
Manufacturer Apex Energetics Inc.
Product type HUMAN OTC DRUG
SPL set ID bed751f5-a8da-cac7-e053-2a95a90a2218
SPL ID 0e767659-f964-7c88-e063-6294a90a0f64
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 03:12:51 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 · 20 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name A13 DTX-LIVER openfda.brand_name generic name BOS TAURUS GALLBLADDER, BRYONIA, CHELIDONIUM MAJUS, CHOLESTERINUM, HEPAR SULPHURIS CALCAREUM , JUNIPERUS COMMUNIS STEM, LYCOPODIUM CLAVATUM, NATRUM SULPHURICUM, PHOSPHORUS, RHAMNUS PURSHIANA, ROSMARINUS OFFICINALIS, SECALE CEREALE WHOLE openfda.generic_name manufacturer name Apex Energetics Inc. openfda.manufacturer_name ndc package 63479-0113-1 openfda.package_ndc ndc product 63479-0113 openfda.product_ndc ndc11 package 63479011301 derived:openfda.package_ndc spl id 0e767659-f964-7c88-e063-6294a90a0f64 id spl set id bed751f5-a8da-cac7-e053-2a95a90a2218 set_id unii 27YLU75U4W openfda.unii unii 7E889U5RNN openfda.unii unii 0YPR65R21J openfda.unii unii 4VBP01X99F openfda.unii unii 8JM482TI79 openfda.unii unii 12M71ST1GZ openfda.unii unii 97C5T2UQ7J openfda.unii unii HBU87MH6OY openfda.unii unii T7J046YI2B openfda.unii unii 9901V1E867 openfda.unii unii C88X29Y479 openfda.unii unii 1MBW07J51Q 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 tiredness, headaches, irritability, muscle pains, poor digestion, skin rash, 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.