Home FDA labels 1fcd3d4a-a24d-41d0-ba2b-4827c04e7c69 Respitory Tonic F 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 Respitory Tonic F
Generic name ECHINACEA (ANGUSTIFOLIA), UVA-URSI, BAPTISIA TINCTORIA, CONVALLARIA MAJALIS, KALI MURIATICUM, PINUS SYLVESTRIS, THUJA OCCIDENTALIS, BRYONIA (ALBA), CONDURANGO, CROTALUS HORRIDUS, GINKGO BILOBA, LACHESIS MUTUS, SELENIUM METALLICUM, TABEBUIA IMPETIGINOSA, VISCUM ALBUM
Manufacturer BioActive Nutritional, Inc.
Product type HUMAN OTC DRUG
SPL set ID 17684967-1e3c-4776-9ae9-d43fa1ebebb1
SPL ID 1fcd3d4a-a24d-41d0-ba2b-4827c04e7c69
Version 3
Effective date 2026-03-09
Source export date 2026-09-28
Source partition 14
Source file https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:40:27 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 · 22 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Respitory Tonic F openfda.brand_name generic name ECHINACEA (ANGUSTIFOLIA), UVA-URSI, BAPTISIA TINCTORIA, CONVALLARIA MAJALIS, KALI MURIATICUM, PINUS SYLVESTRIS, THUJA OCCIDENTALIS, BRYONIA (ALBA), CONDURANGO, CROTALUS HORRIDUS, GINKGO BILOBA, LACHESIS MUTUS, SELENIUM METALLICUM, TABEBUIA IMPETIGINOSA, VISCUM ALBUM openfda.generic_name manufacturer name BioActive Nutritional, Inc. openfda.manufacturer_name ndc package 43857-0583-1 openfda.package_ndc ndc product 43857-0583 openfda.product_ndc ndc11 package 43857058301 derived:openfda.package_ndc spl id 1fcd3d4a-a24d-41d0-ba2b-4827c04e7c69 id spl set id 17684967-1e3c-4776-9ae9-d43fa1ebebb1 set_id unii QHH4HVF5QE openfda.unii unii 1NT28V9397 openfda.unii unii VB06AV5US8 openfda.unii unii Q1RGP4UB73 openfda.unii unii 660YQ98I10 openfda.unii unii 3M5V3D1X36 openfda.unii unii T7J046YI2B openfda.unii unii VSW71SS07I openfda.unii unii 19FUJ2C58T openfda.unii unii BK9092J5MP openfda.unii unii 5EF0HWI5WU openfda.unii unii YHA2XLJ956 openfda.unii unii 6GLA1946WX openfda.unii unii H6241UJ22B 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 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.