Home FDA labels 050da0b7-7d13-47a4-b3a0-dd3830c0e998 LD Force HP 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 LD Force HP
Generic name ARSENICUM ALBUM, BORRELIA BURGDORFERI NOSODE, CHELIDONIUM MAJUS, COCCUS CACTI, ECHINACEA (ANGUSTIFOLIA), HYDRASTIS CANADENSIS, LYCOPODIUM CLAVATUM, NASTURTIUM AQUATICUM, PHOSPHORUS, RHUS TOX, TARAXACUM OFFICINALE, THYMUS (SUIS), THYROIDINUM (SUIS), TRIFOLIUM PRATENSE, URTICA DIOICA
Manufacturer BioActive Nutritional, Inc.
Product type HUMAN OTC DRUG
SPL set ID 40016043-bd05-4ef2-b44b-ad73879815a1
SPL ID 050da0b7-7d13-47a4-b3a0-dd3830c0e998
Version 2
Effective date 2024-10-17
Source export date 2026-10-12
Source partition 12
Source file https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:56:26 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name LD Force HP openfda.brand_name generic name ARSENICUM ALBUM, BORRELIA BURGDORFERI NOSODE, CHELIDONIUM MAJUS, COCCUS CACTI, ECHINACEA (ANGUSTIFOLIA), HYDRASTIS CANADENSIS, LYCOPODIUM CLAVATUM, NASTURTIUM AQUATICUM, PHOSPHORUS, RHUS TOX, TARAXACUM OFFICINALE, THYMUS (SUIS), THYROIDINUM (SUIS), TRIFOLIUM PRATENSE, URTICA DIOICA openfda.generic_name manufacturer name BioActive Nutritional, Inc. openfda.manufacturer_name ndc package 43857-0618-1 openfda.package_ndc ndc product 43857-0618 openfda.product_ndc ndc11 package 43857061801 derived:openfda.package_ndc spl id 050da0b7-7d13-47a4-b3a0-dd3830c0e998 id spl set id 40016043-bd05-4ef2-b44b-ad73879815a1 set_id unii 27YLU75U4W openfda.unii unii 6RV024OAUQ openfda.unii unii 7E889U5RNN openfda.unii unii 710FLW4U46 openfda.unii unii LZB7TFX1LT openfda.unii unii 39981FM375 openfda.unii unii 7B69B0BD62 openfda.unii unii 6IO182RP7A openfda.unii unii S7V92P67HO openfda.unii unii VB06AV5US8 openfda.unii unii ZW3Z11D0JV openfda.unii unii YH89GMV676 openfda.unii unii 4JS0838828 openfda.unii unii C88X29Y479 openfda.unii unii 0J8NV9V5Q8 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 cool, dry place.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.