Home FDA labels 0e76df45-c9e8-7085-e063-6294a90a6423 D07 LMPH-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 D07 LMPH-DRN
Generic name ARANEUS DIADEMATUS, ARISAEMA TRIPHYLLUM ROOT, ASTERIAS RUBENS, BAPTISIA TINCTORIA, BARIUM IODIDE, ECHINACEA ANGUSTIFOLIA, FERROUS IODIDE, GOLDENSEAL, LACHESIS MUTA VENOM, PHYTOLACCA AMERICANA ROOT, PINUS SYLVESTRIS FLOWERING TOP, SCROPHULARIA NODOSA, SPONGIA OFFICINALIS SKELETON, ROASTED, AND TEUCRIUM SCORODONIA FLOWERING TOP
Manufacturer Apex Energetics Inc.
Product type HUMAN OTC DRUG
SPL set ID c287b39d-d0cd-4e5d-8930-6f07f2ed89de
SPL ID 0e76df45-c9e8-7085-e063-6294a90a6423
Version 5
Effective date 2024-01-08
Source export date 2026-11-06
Source partition 5
Source file https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-11-06/f699a9578a0c5d6f5abd59491e85ce3c2c5e4567a51003fee350566c56ba5812/drug-label-0005-of-0014.json.zip
Source manifest SHA-256 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run 20261106T075659Z
Imported at 2026-11-06 08:29:32 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 D07 LMPH-DRN openfda.brand_name generic name ARANEUS DIADEMATUS, ARISAEMA TRIPHYLLUM ROOT, ASTERIAS RUBENS, BAPTISIA TINCTORIA, BARIUM IODIDE, ECHINACEA ANGUSTIFOLIA, FERROUS IODIDE, GOLDENSEAL, LACHESIS MUTA VENOM, PHYTOLACCA AMERICANA ROOT, PINUS SYLVESTRIS FLOWERING TOP, SCROPHULARIA NODOSA, SPONGIA OFFICINALIS SKELETON, ROASTED, AND TEUCRIUM SCORODONIA FLOWERING TOP openfda.generic_name manufacturer name Apex Energetics Inc. openfda.manufacturer_name ndc package 63479-0407-1 openfda.package_ndc ndc product 63479-0407 openfda.product_ndc ndc11 package 63479040701 derived:openfda.package_ndc spl id 0e76df45-c9e8-7085-e063-6294a90a6423 id spl set id c287b39d-d0cd-4e5d-8930-6f07f2ed89de set_id unii 11E6VI8VEG openfda.unii unii 2HEM73YI9I openfda.unii unii 6T6CO7R3Z5 openfda.unii unii VB06AV5US8 openfda.unii unii A7FYY9Q742 openfda.unii unii WKC4T7680A openfda.unii unii ZW3Z11D0JV openfda.unii unii VSW71SS07I openfda.unii unii 1PIP394IID openfda.unii unii 5EF0HWI5WU openfda.unii unii LOK3I16O7G openfda.unii unii F5452U54PN openfda.unii unii DM64K844DM openfda.unii unii 7H443NUB2T 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 breast-feeding , 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 congestion, headache, fatigue, loss of appetite, itchy skin, 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.