Home FDA labels 8d05c176-2973-4040-9a45-53872bf94f92 Fungus Nosode 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 Fungus Nosode
Generic name ACHORION SCHO, ALTERNARIA ALT, ASPERGILLUS FUM, ASPERGILLUS NIGER, BOLETUS SAT, BOTRYTIS CIN, CANDIDA PARAP, CLADOSPORIUM MET, FUSARIUM OXY, HELMINTHOSPORIUM SAT, MICROSPORON FUR, MUCOR MUECEDO, PULLULARIA PULL, RHIZOPUS NIG, SACCHAROMYCES CER, TRICHOPHYTON SPP, USTILAGO MAYDIS
Manufacturer Natural Creations, Inc
Product type HUMAN OTC DRUG
SPL set ID 2013d9d2-3237-4899-8a2f-4ef89555ed9b
SPL ID 8d05c176-2973-4040-9a45-53872bf94f92
Version 2
Effective date 2025-12-10
Source export date 2026-10-12
Source partition 8
Source file https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:14:42 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 Fungus Nosode openfda.brand_name generic name ACHORION SCHO, ALTERNARIA ALT, ASPERGILLUS FUM, ASPERGILLUS NIGER, BOLETUS SAT, BOTRYTIS CIN, CANDIDA PARAP, CLADOSPORIUM MET, FUSARIUM OXY, HELMINTHOSPORIUM SAT, MICROSPORON FUR, MUCOR MUECEDO, PULLULARIA PULL, RHIZOPUS NIG, SACCHAROMYCES CER, TRICHOPHYTON SPP, USTILAGO MAYDIS openfda.generic_name manufacturer name Natural Creations, Inc openfda.manufacturer_name ndc package 43406-0120-1 openfda.package_ndc ndc product 43406-0120 openfda.product_ndc ndc11 package 43406012001 derived:openfda.package_ndc spl id 8d05c176-2973-4040-9a45-53872bf94f92 id spl set id 2013d9d2-3237-4899-8a2f-4ef89555ed9b set_id unii Z4MD1809H1 openfda.unii unii 4K7Z7K7SWG openfda.unii unii 68OG1407SM openfda.unii unii D1A2NG69CK openfda.unii unii R0AD5705HC openfda.unii unii 5398RXP8KU openfda.unii unii 3LN5B70U4W openfda.unii unii TBW53313S7 openfda.unii unii 6JR6JTN25S openfda.unii unii FEE198DK4Q openfda.unii unii 0KZ676D44N openfda.unii unii 52B29REC7H openfda.unii unii J17GBZ5VGX openfda.unii unii 9IOA40ANG6 openfda.unii unii X88DF51T48 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: Consult a physician for use in children under 12 years of age. IF PREGNANT OR BREAST-FEEDING , ask a health care professional before use. KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away. Do not use if TAMPER EVIDENT seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.