Home FDA labels 132d6703-451f-4dca-b1bc-997c667354d1 OHM-INMA 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 OHM-INMA
Generic name ACONITUM NAPELLUS, ARANEA DIADEMA, ARNICA MONTANA, ASCLEPIAS VINCETOXICUM, BAPTISIA TINCTORIA, BRYONIA ALBA, ECHINACEA ANGUSTIFOLIA, EQUISETUM HYEMALE, EUPATORIUM PERFORLIATUM, GELSEMIUM SEMPERVIRENS, HEPAR SULPHURIS CALCAREUM, JUGLANS REGIA, PHYTOLACCA DECANDRA, SANGUINARIA CANADENSIS, SARSAPARILLA, SULPHUR, ZINCUM METALLICUM
Manufacturer OHM PHARMA INC.
Product type HUMAN PRESCRIPTION DRUG
SPL set ID bc8e72c7-b7e6-4d5d-bd37-75202244d440
SPL ID 132d6703-451f-4dca-b1bc-997c667354d1
Version 2
Effective date 2021-03-25
Source export date 2026-10-12
Source partition 11
Source file https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:44:36 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 · 25 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name OHM-INMA openfda.brand_name generic name ACONITUM NAPELLUS, ARANEA DIADEMA, ARNICA MONTANA, ASCLEPIAS VINCETOXICUM, BAPTISIA TINCTORIA, BRYONIA ALBA, ECHINACEA ANGUSTIFOLIA, EQUISETUM HYEMALE, EUPATORIUM PERFORLIATUM, GELSEMIUM SEMPERVIRENS, HEPAR SULPHURIS CALCAREUM, JUGLANS REGIA, PHYTOLACCA DECANDRA, SANGUINARIA CANADENSIS, SARSAPARILLA, SULPHUR, ZINCUM METALLICUM openfda.generic_name manufacturer name OHM PHARMA INC. openfda.manufacturer_name ndc package 66096-757-02 openfda.package_ndc ndc product 66096-757 openfda.product_ndc ndc11 package 66096075702 derived:openfda.package_ndc spl id 132d6703-451f-4dca-b1bc-997c667354d1 id spl set id bc8e72c7-b7e6-4d5d-bd37-75202244d440 set_id unii 11E6VI8VEG openfda.unii unii O80TY208ZW openfda.unii unii 5K1UO2888Y openfda.unii unii 2H1576D5WG openfda.unii unii 639KR60Q1Q openfda.unii unii 6T6CO7R3Z5 openfda.unii unii VB06AV5US8 openfda.unii unii 59677RXH25 openfda.unii unii T7J046YI2B openfda.unii unii 70FD1KFU70 openfda.unii unii U0NQ8555JD openfda.unii unii 1W0775VX6E openfda.unii unii 85HKB87105 openfda.unii unii N9288CD508 openfda.unii unii J41CSQ7QDS openfda.unii unii 1MBW07J51Q openfda.unii unii 9R858U917W 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 Advertencias: Venta bajo prescripción médica, mantengase fuera del alcance de los niños. No utilizar si el sello de seguridad del spray esta roto. Mantener el medicamento protegido del calor, luz y humedad, almacenar a no más de 30°C. Mantengase fuera del alcance de los niños.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.