Home FDA labels 39583480-a1ae-4e26-a9be-cfe57922ebf7 Respiforce A 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 A
Generic name ARNICA MONTANA, ASCLEPIAS TUBEROSA, ERIODICTYON CALIFORNICUM, EUCALYPTUS GLOBULUS, LOBELIA INFLATA, PLANTAGO MAJOR, TRIFOLIUM PRATENSE, ARSENICUM ALBUM, BELLADONNA, BRYONIA, CARBO VEGETABILIS, GRINDELIA, KALI CARBONICUM, NATRUM SULPHURICUM, PULSATILLA,
Manufacturer BioActive Nutritional
Product type HUMAN OTC DRUG
SPL set ID e9360698-bffb-4c91-b019-22e1e56704ee
SPL ID 39583480-a1ae-4e26-a9be-cfe57922ebf7
Version 3
Effective date 2025-04-02
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 06:07:21 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 Respiforce A openfda.brand_name generic name ARNICA MONTANA, ASCLEPIAS TUBEROSA, ERIODICTYON CALIFORNICUM, EUCALYPTUS GLOBULUS, LOBELIA INFLATA, PLANTAGO MAJOR, TRIFOLIUM PRATENSE, ARSENICUM ALBUM, BELLADONNA, BRYONIA, CARBO VEGETABILIS, GRINDELIA, KALI CARBONICUM, NATRUM SULPHURICUM, PULSATILLA, openfda.generic_name manufacturer name BioActive Nutritional openfda.manufacturer_name ndc package 43857-0599-1 openfda.package_ndc ndc product 43857-0599 openfda.product_ndc ndc11 package 43857059901 derived:openfda.package_ndc spl id 39583480-a1ae-4e26-a9be-cfe57922ebf7 id spl set id e9360698-bffb-4c91-b019-22e1e56704ee set_id unii 2P3VWU3H10 openfda.unii unii 1ZL82U5D18 openfda.unii unii 9PP1T3TC5U openfda.unii unii O80TY208ZW openfda.unii unii 0YPR65R21J openfda.unii unii 2Y7TIQ135H openfda.unii unii BQN1B9B9HA openfda.unii unii W2469WNO6U openfda.unii unii S7V92P67HO openfda.unii unii WQZ3G9PF0H openfda.unii unii T7J046YI2B openfda.unii unii IDB0NAZ6AI openfda.unii unii 4JS0838828 openfda.unii unii I76KB35JEV 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 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.