Home FDA labels 0e76e634-d93f-70ac-e063-6294a90a6ad3 D01 DRAINAGE COMPLEX 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 D01 DRAINAGE COMPLEX
Generic name ALFALFA, ALLIUM SATIVUM, ASPARAGUS OFFICINALIS, AVENA SATIVA, BELLADONNA, BERBERIS VULGARIS, CHELIDONIUM MAJUS, GLYCYRRHIZA GLABRA, HYDRASTIS CANADENSIS, JUNIPERUS VIRGINIANA, NICCOLUM METALLICUM, PASSIFLORA INCARNATA, SARCOLACTICUM ACIDUM, SOLIDAGO VIRGAUREA, TARAXACUM OFFICINALE
Manufacturer Apex Energetics Inc.
Product type HUMAN OTC DRUG
SPL set ID ba7020bf-3fc5-4fbf-e053-2995a90a70d7
SPL ID 0e76e634-d93f-70ac-e063-6294a90a6ad3
Version 2
Effective date 2024-01-08
Source export date 2026-09-28
Source partition 3
Source file https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:19:33 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 D01 DRAINAGE COMPLEX openfda.brand_name generic name ALFALFA, ALLIUM SATIVUM, ASPARAGUS OFFICINALIS, AVENA SATIVA, BELLADONNA, BERBERIS VULGARIS, CHELIDONIUM MAJUS, GLYCYRRHIZA GLABRA, HYDRASTIS CANADENSIS, JUNIPERUS VIRGINIANA, NICCOLUM METALLICUM, PASSIFLORA INCARNATA, SARCOLACTICUM ACIDUM, SOLIDAGO VIRGAUREA, TARAXACUM OFFICINALE openfda.generic_name manufacturer name Apex Energetics Inc. openfda.manufacturer_name ndc package 63479-0401-1 openfda.package_ndc ndc product 63479-0401 openfda.product_ndc ndc11 package 63479040101 derived:openfda.package_ndc spl id 0e76e634-d93f-70ac-e063-6294a90a6ad3 id spl set id ba7020bf-3fc5-4fbf-e053-2995a90a70d7 set_id unii V1V998DC17 openfda.unii unii 7E889U5RNN openfda.unii unii 2788Z9758H openfda.unii unii DJO934BRBD openfda.unii unii Z1EJP3037Z openfda.unii unii 1TH8Q20J0U openfda.unii unii 39981FM375 openfda.unii unii F9S9FFU82N openfda.unii unii 532BCG080L openfda.unii unii ZW3Z11D0JV openfda.unii unii WQZ3G9PF0H openfda.unii unii 7OV03QG267 openfda.unii unii MA9CQJ3F7F openfda.unii unii CLF5YFS11O 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 tiredness, irritability, muscle cramps, headache, sleeplessness, restlessness, 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.