Home FDA labels 6c5dccbb-ed1b-40b8-997a-b870288ee01e Scrofularoforce 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 Scrofularoforce
Generic name RUMEX CRISPUS, XANTHOXYLUM FRAXINEUM, LYMPH NODE (SUIS), SCROPHULARIA NODOSA, BARYTA CARBONICA, BARYTA MURIATICA, BELLADONNA, CALCAREA CARBONICA, CONIUM MACULATUM, HELLEBORUS NIGER, IODIUM, KALI PHOSPHORICUM, LACHESIS MUTUS, NATRUM PHOSPHORICUM, SILICEA, JUNIPERUS VIRGINIANA
Manufacturer BioActive Nutritional, Inc.
Product type HUMAN OTC DRUG
SPL set ID 737cd410-0405-41b0-b7f2-29bb20037849
SPL ID 6c5dccbb-ed1b-40b8-997a-b870288ee01e
Version 3
Effective date 2026-06-08
Source export date 2026-10-12
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/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:32:32 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 Scrofularoforce openfda.brand_name generic name RUMEX CRISPUS, XANTHOXYLUM FRAXINEUM, LYMPH NODE (SUIS), SCROPHULARIA NODOSA, BARYTA CARBONICA, BARYTA MURIATICA, BELLADONNA, CALCAREA CARBONICA, CONIUM MACULATUM, HELLEBORUS NIGER, IODIUM, KALI PHOSPHORICUM, LACHESIS MUTUS, NATRUM PHOSPHORICUM, SILICEA, JUNIPERUS VIRGINIANA openfda.generic_name manufacturer name BioActive Nutritional, Inc. openfda.manufacturer_name ndc package 43857-0580-1 openfda.package_ndc ndc product 43857-0580 openfda.product_ndc ndc11 package 43857058001 derived:openfda.package_ndc spl id 6c5dccbb-ed1b-40b8-997a-b870288ee01e id spl set id 737cd410-0405-41b0-b7f2-29bb20037849 set_id unii CI71S98N1Z openfda.unii unii A4KL1HMZ7T openfda.unii unii Q28R5GF371 openfda.unii unii EL5GJ3U77E openfda.unii unii 608DGJ6815 openfda.unii unii 6P669D8HQ8 openfda.unii unii 33A7VYU29L openfda.unii unii 9679TC07X4 openfda.unii unii 9N1RM2S62C openfda.unii unii ETJ7Z6XBU4 openfda.unii unii 2E32821G6I openfda.unii unii 532BCG080L openfda.unii unii WQZ3G9PF0H openfda.unii unii VSW71SS07I openfda.unii unii 70WT22SF4B 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 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.