Home FDA labels 36c231fe-47b6-47e5-8f89-7de6c22b7ccb Edemaforce 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 Edemaforce
Generic name CACTUS GRANDIFLORUS, CALENDULA OFFICINALIS, DULCAMARA, LEPTANDRA VIRGINICA, SOLIDAGO VIRGAUREA, CONVALLARIA MAJALIS, APIS MELLIFICA, ARNICA MONTANA, BERBERIS VULGARIS, BRYONIA (ALBA), CHELIDONIUM MAJUS, LYCOPODIUM CLAVATUM, PLUMBUM METALLICUM, SAMBUCUS NIGRA
Manufacturer BioActive Nutritional, Inc.
Product type HUMAN OTC DRUG
SPL set ID 5e7d1909-932a-41a3-bad3-be320bb9ef35
SPL ID 36c231fe-47b6-47e5-8f89-7de6c22b7ccb
Version 2
Effective date 2026-08-20
Source export date 2026-09-28
Source partition 11
Source file https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:18:27 Harmonized routes table Harmonized routes ORAL
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 Edemaforce openfda.brand_name generic name CACTUS GRANDIFLORUS, CALENDULA OFFICINALIS, DULCAMARA, LEPTANDRA VIRGINICA, SOLIDAGO VIRGAUREA, CONVALLARIA MAJALIS, APIS MELLIFICA, ARNICA MONTANA, BERBERIS VULGARIS, BRYONIA (ALBA), CHELIDONIUM MAJUS, LYCOPODIUM CLAVATUM, PLUMBUM METALLICUM, SAMBUCUS NIGRA openfda.generic_name manufacturer name BioActive Nutritional, Inc. openfda.manufacturer_name ndc package 43857-0395-1 openfda.package_ndc ndc product 43857-0395 openfda.product_ndc ndc11 package 43857039501 derived:openfda.package_ndc spl id 36c231fe-47b6-47e5-8f89-7de6c22b7ccb id spl set id 5e7d1909-932a-41a3-bad3-be320bb9ef35 set_id unii 7E889U5RNN openfda.unii unii KPS1B1162N openfda.unii unii O80TY208ZW openfda.unii unii 18E7415PXQ openfda.unii unii 1TH8Q20J0U openfda.unii unii QHH4HVF5QE openfda.unii unii M2O62YTN42 openfda.unii unii T7J046YI2B openfda.unii unii 2P299V784P openfda.unii unii CT03BSA18U openfda.unii unii 7S82P3R43Z openfda.unii unii 5405K23S50 openfda.unii unii C88X29Y479 openfda.unii unii 7114SV0MYK 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 care professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.