Home FDA labels b7302af9-48c6-413a-b0c9-dd7a468c9f3a Triple Flu Defense 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 Triple Flu Defense
Generic name ACONITUM NAPELLUS, ANAS BARBARIAE, HEPATIS ET CORDIS EXTRACTUM, BRYONIA (ALBA), EUPATORIUM PERFOLIATUM, GELSEMIUM SEMPERVIRENS, INFLUENZINUM, IPECACUANHA, NUX VOMICA, PHOSPHORUS, PHYTOLACCA DECANDRA, SANGUINARIA CANADENSIS, STICTA PULMONARIA
Manufacturer Nenningers Naturals
Product type HUMAN OTC DRUG
SPL set ID 04889636-6e05-4d9c-aaba-194251adfa31
SPL ID b7302af9-48c6-413a-b0c9-dd7a468c9f3a
Version 3
Effective date 2026-05-06
Source export date 2026-10-12
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/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 03:12:59 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 Triple Flu Defense openfda.brand_name generic name ACONITUM NAPELLUS, ANAS BARBARIAE, HEPATIS ET CORDIS EXTRACTUM, BRYONIA (ALBA), EUPATORIUM PERFOLIATUM, GELSEMIUM SEMPERVIRENS, INFLUENZINUM, IPECACUANHA, NUX VOMICA, PHOSPHORUS, PHYTOLACCA DECANDRA, SANGUINARIA CANADENSIS, STICTA PULMONARIA openfda.generic_name manufacturer name Nenningers Naturals openfda.manufacturer_name ndc package 42731-082-01 openfda.package_ndc ndc product 42731-082 openfda.product_ndc ndc11 package 42731008201 derived:openfda.package_ndc spl id b7302af9-48c6-413a-b0c9-dd7a468c9f3a id spl set id 04889636-6e05-4d9c-aaba-194251adfa31 set_id unii 27YLU75U4W openfda.unii unii 11E6VI8VEG openfda.unii unii PS2DCE2WVF openfda.unii unii 269XH13919 openfda.unii unii R9HH0NDE2E openfda.unii unii 639KR60Q1Q openfda.unii unii CYK5P89K8X openfda.unii unii 62I3C8233L openfda.unii unii T7J046YI2B openfda.unii unii RN2HC612GY openfda.unii unii U0NQ8555JD openfda.unii unii 1W0775VX6E openfda.unii unii N9288CD508 openfda.unii unii PMY5J4Z7LS openfda.unii unii D1YM0P5Z2T 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 that 2 days or administer to children under 3 years of age unless directed by physician. If symptoms worsen or persist for more than 3 days consult a doctor. If Pregnant or breastfeeding consult a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Use only if safety seal is intact. Store at room temperature.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.