Home FDA labels 6f16f1eb-457d-44db-9f7a-9d9364010b20 Respiforce I 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 Respiforce I
Generic name ECHINACEA (ANGUSTIFOLIA), LOMATIUM DISSECTUM, MYRRHA, NASTURTIUM AQUATICUM, TABEBUIA IMPETIGINOSA, HYDRASTIS CANADENSIS, PROPOLIS, BRYONIA (ALBA), EUPATORIUM PERFOLIATUM, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, IPECACUANHA, MERCURIUS CORROSIVUS, PYROGENIUM, INFLUENZINUM
Manufacturer BioActive Nutritional, Inc.
Product type HUMAN OTC DRUG
SPL set ID 7dca20cc-91ae-4f20-896d-10365b82711b
SPL ID 6f16f1eb-457d-44db-9f7a-9d9364010b20
Version 1
Effective date 2025-12-30
Source export date 2026-09-28
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:07:27 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 · 26 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Respiforce I openfda.brand_name generic name ECHINACEA (ANGUSTIFOLIA), LOMATIUM DISSECTUM, MYRRHA, NASTURTIUM AQUATICUM, TABEBUIA IMPETIGINOSA, HYDRASTIS CANADENSIS, PROPOLIS, BRYONIA (ALBA), EUPATORIUM PERFOLIATUM, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, IPECACUANHA, MERCURIUS CORROSIVUS, PYROGENIUM, INFLUENZINUM openfda.generic_name manufacturer name BioActive Nutritional, Inc. openfda.manufacturer_name ndc package 43857-0661-1 openfda.package_ndc ndc product 43857-0661 openfda.product_ndc ndc11 package 43857066101 derived:openfda.package_ndc spl id 6f16f1eb-457d-44db-9f7a-9d9364010b20 id spl set id 7dca20cc-91ae-4f20-896d-10365b82711b set_id unii PS2DCE2WVF openfda.unii unii 639KR60Q1Q openfda.unii unii 29SUH5R3HU openfda.unii unii 53GH7MZT1R openfda.unii unii AU5C98U4BB openfda.unii unii 91GQH8I5F7 openfda.unii unii VB06AV5US8 openfda.unii unii 6Y8XYV2NOF openfda.unii unii CYK5P89K8X openfda.unii unii ZW3Z11D0JV openfda.unii unii 5329928G5N openfda.unii unii 62I3C8233L openfda.unii unii T7J046YI2B openfda.unii unii 1W0775VX6E openfda.unii unii YH89GMV676 openfda.unii unii 6GLA1946WX openfda.unii unii 6TU4EY6UNW openfda.unii unii JC71GJ1F3L 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: Sore Throat Warning Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult physician promptly. Do not use more than 2 days or administer to children under 3 years of age unless directed by a physician. 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.