Home FDA labels 0e76ea05-c3d0-8465-e063-6294a90a747f D03 LVR-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 D03 LVR-DRN
Generic name BERBERIS VULGARIS ROOT BARK, BRYONIA ALBA ROOT, PHENOL, MILK THISTLE, CHELIDONIUM MAJUS, JUNIPER BERRY, LYCOPODIUM CLAVATUM SPORE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, SODIUM SULFATE, STRYCHNOS NUX-VOMICA SEED, PHOSPHORUS, LACTIC ACID, L-, TARAXACUM OFFICINALE, VISCUM ALBUM FRUITING TOP, AND YUCCA FILAMENTOSA
Manufacturer Apex Energetics Inc.
Product type HUMAN OTC DRUG
SPL set ID f7eba30d-04f6-43b6-9020-052f1207e9f2
SPL ID 0e76ea05-c3d0-8465-e063-6294a90a747f
Version 4
Effective date 2024-01-08
Source export date 2026-10-27
Source partition 7
Source file https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
Source manifest SHA-256 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run 20261027T193451Z
Imported at 2026-10-27 20:15:26 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 D03 LVR-DRN openfda.brand_name generic name BERBERIS VULGARIS ROOT BARK, BRYONIA ALBA ROOT, PHENOL, MILK THISTLE, CHELIDONIUM MAJUS, JUNIPER BERRY, LYCOPODIUM CLAVATUM SPORE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, SODIUM SULFATE, STRYCHNOS NUX-VOMICA SEED, PHOSPHORUS, LACTIC ACID, L-, TARAXACUM OFFICINALE, VISCUM ALBUM FRUITING TOP, AND YUCCA FILAMENTOSA openfda.generic_name manufacturer name Apex Energetics Inc. openfda.manufacturer_name ndc package 63479-0403-1 openfda.package_ndc ndc product 63479-0403 openfda.product_ndc ndc11 package 63479040301 derived:openfda.package_ndc spl id 0e76ea05-c3d0-8465-e063-6294a90a747f id spl set id f7eba30d-04f6-43b6-9020-052f1207e9f2 set_id unii 27YLU75U4W openfda.unii unii 7E889U5RNN openfda.unii unii 269XH13919 openfda.unii unii 0YPR65R21J openfda.unii unii 1TH8Q20J0U openfda.unii unii 39981FM375 openfda.unii unii U946SH95EE openfda.unii unii F9S9FFU82N openfda.unii unii 339NCG44TV openfda.unii unii T7J046YI2B openfda.unii unii T6VR38UJ9I openfda.unii unii O84B5194RL openfda.unii unii BK9092J5MP openfda.unii unii 70WT22SF4B openfda.unii unii C88X29Y479 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: 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 fatigue, headache, muscle ache, nervous irritability, restlessness, difficulty sleeping, 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.