Home FDA labels 452d9c3d-c9f9-45e7-bf5e-c91feb012c73 FNG II 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 FNG II
Generic name ECHINACEA (ANGUSTIFOLIA), LOMATIUM DISSECTUM, NASTURTIUM AQUATICUM, TABEBUIA IMPETIGINOSA, HYDRASTIS CANADENSIS, IODIUM, ADRENALINUM, ARGENTUM METALLICUM, THYMUS (SUIS), THYROIDINUM (SUIS), PHOSPHORICUM ACIDUM, CANDIDA ALBICANS, LYCOPODIUM CLAVATUM, PULSATILLA (VULGARIS), SEPIA
Manufacturer BioActive Nutritional, Inc.
Product type HUMAN OTC DRUG
SPL set ID d15cbfe9-051d-4aeb-a0f3-105bef7796bc
SPL ID 452d9c3d-c9f9-45e7-bf5e-c91feb012c73
Version 3
Effective date 2026-05-07
Source export date 2026-09-28
Source partition 2
Source file https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:15:19 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 FNG II openfda.brand_name generic name ECHINACEA (ANGUSTIFOLIA), LOMATIUM DISSECTUM, NASTURTIUM AQUATICUM, TABEBUIA IMPETIGINOSA, HYDRASTIS CANADENSIS, IODIUM, ADRENALINUM, ARGENTUM METALLICUM, THYMUS (SUIS), THYROIDINUM (SUIS), PHOSPHORICUM ACIDUM, CANDIDA ALBICANS, LYCOPODIUM CLAVATUM, PULSATILLA (VULGARIS), SEPIA openfda.generic_name manufacturer name BioActive Nutritional, Inc. openfda.manufacturer_name ndc package 43857-0424-1 openfda.package_ndc ndc product 43857-0424 openfda.product_ndc ndc11 package 43857042401 derived:openfda.package_ndc spl id 452d9c3d-c9f9-45e7-bf5e-c91feb012c73 id spl set id d15cbfe9-051d-4aeb-a0f3-105bef7796bc set_id unii 6RV024OAUQ openfda.unii unii 3M4G523W1G openfda.unii unii QDL83WN8C2 openfda.unii unii 9679TC07X4 openfda.unii unii 4D7G21HDBC openfda.unii unii 7B69B0BD62 openfda.unii unii YKH834O4BH openfda.unii unii VB06AV5US8 openfda.unii unii ZW3Z11D0JV openfda.unii unii 5329928G5N openfda.unii unii E4GA8884NN openfda.unii unii YH89GMV676 openfda.unii unii 6GLA1946WX openfda.unii unii I76KB35JEV openfda.unii unii C88X29Y479 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.