Home FDA labels 2d52d5ef-5023-40d2-9ff4-0fd277db68ec Cardioforce I 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 Cardioforce I
Generic name ARNICA MONTANA, CACTUS GRANDIFLORUS, CAPSICUM ANNUUM, DIGITALIS PURPUREA, KALI PHOSPHORICUM, LAUROCERASUS, SPIGELIA ANTHELMIA, TABACUM, ACONITUM NAPELLUS, AGARICUS MUSCARIUS, AURUM MURIATICUM, GLONOINUM, IGNATIA AMARA, KALMIA LATIFOLIA, LATRODECTUS MACTANS, VALERIANA OFFICINALIS
Manufacturer BioActive Nutritional, Inc.
Product type HUMAN OTC DRUG
SPL set ID 0bb404b6-a7c1-4077-995e-d7ce59409a29
SPL ID 2d52d5ef-5023-40d2-9ff4-0fd277db68ec
Version 2
Effective date 2024-10-17
Source export date 2026-10-27
Source partition 6
Source file https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-27/55ffdfed5c29f1b4aed512886bd3fb7831e157cc4948137779971a558752ed2b/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run 20261027T193451Z
Imported at 2026-10-27 20:07:22 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 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Cardioforce I openfda.brand_name generic name ARNICA MONTANA, CACTUS GRANDIFLORUS, CAPSICUM ANNUUM, DIGITALIS PURPUREA, KALI PHOSPHORICUM, LAUROCERASUS, SPIGELIA ANTHELMIA, TABACUM, ACONITUM NAPELLUS, AGARICUS MUSCARIUS, AURUM MURIATICUM, GLONOINUM, IGNATIA AMARA, KALMIA LATIFOLIA, LATRODECTUS MACTANS, VALERIANA OFFICINALIS openfda.generic_name manufacturer name BioActive Nutritional, Inc. openfda.manufacturer_name ndc package 43857-0442-1 openfda.package_ndc ndc product 43857-0442 openfda.product_ndc ndc11 package 43857044201 derived:openfda.package_ndc spl id 2d52d5ef-5023-40d2-9ff4-0fd277db68ec id spl set id 0bb404b6-a7c1-4077-995e-d7ce59409a29 set_id unii 00UK7646FG openfda.unii unii CI71S98N1Z openfda.unii unii O80TY208ZW openfda.unii unii 79N6542N18 openfda.unii unii 15443PR153 openfda.unii unii F26P2D4757 openfda.unii unii DIF093I037 openfda.unii unii 6YR2608RSU openfda.unii unii 1NM3M2487K openfda.unii unii XJJ7QA858R openfda.unii unii WYT05213GE openfda.unii unii JWF5YAW3QW openfda.unii unii U0NQ8555JD openfda.unii unii G59M7S0WS3 openfda.unii unii F1T8QT9U8B 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.