Home FDA labels bdfd4d37-8af9-40a8-bb69-8eb95c1c1024 Inflammation 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 Inflammation
Generic name APIS MELLIFICA, ARNICA MONTANA, BAPTISIA TINCTORIA, BENZOICUM ACIDUM, BRYONIA (ALBA), COLCHICUM AUTUMNALE, DULCAMARA, ECHINACEA (ANGUSTIFOLIA), EUCALYPTUS GLOBULUS, EUPATORIUM PERFOLIATUM, MERCURIALIS PERENNIS, RHUS TOX, SOLANUM NIGRUM
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID e53db678-6924-41b6-ad7e-32e40d7ee785
SPL ID bdfd4d37-8af9-40a8-bb69-8eb95c1c1024
Version 1
Effective date 2024-04-08
Source export date 2026-09-28
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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:55:59 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 · 21 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Inflammation openfda.brand_name generic name APIS MELLIFICA, ARNICA MONTANA, BAPTISIA TINCTORIA, BENZOICUM ACIDUM, BRYONIA (ALBA), COLCHICUM AUTUMNALE, DULCAMARA, ECHINACEA (ANGUSTIFOLIA), EUCALYPTUS GLOBULUS, EUPATORIUM PERFOLIATUM, MERCURIALIS PERENNIS, RHUS TOX, SOLANUM NIGRUM openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-2112-1 openfda.package_ndc ndc product 43742-2112 openfda.product_ndc ndc11 package 43742211201 derived:openfda.package_ndc spl id bdfd4d37-8af9-40a8-bb69-8eb95c1c1024 id spl set id e53db678-6924-41b6-ad7e-32e40d7ee785 set_id unii 993QHL78E6 openfda.unii unii KPS1B1162N openfda.unii unii O80TY208ZW openfda.unii unii 8SKN0B0MIM openfda.unii unii 0FMD6WV47M openfda.unii unii 6IO182RP7A openfda.unii unii VB06AV5US8 openfda.unii unii T7J046YI2B openfda.unii unii Q35465A1MA openfda.unii unii 1W0775VX6E openfda.unii unii 5EF0HWI5WU openfda.unii unii 7S82P3R43Z openfda.unii unii S546YLW6E6 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 professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.