Home FDA labels 104b8848-918c-4e72-b2cb-254539b50cec 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, ANTIMONIUM CRUDUM, BRYONIA (ALBA), EUPATORIUM PERFOLIATUM, GELSEMIUM SEMPERVIRENS, INFLUENZINUM, IPECACUANHA, KALI BICHROMICUM, NUX VOMICA, PHOSPHORUS, PHYTOLACCA DECANDRA
Manufacturer Nenningers Naturals, LLC
Product type HUMAN OTC DRUG
SPL set ID 43bbed35-e351-409a-b6b6-7da1959634bf
SPL ID 104b8848-918c-4e72-b2cb-254539b50cec
Version 1
Effective date 2025-11-25
Source export date 2026-09-28
Source partition 12
Source file https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:27:59 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, ANTIMONIUM CRUDUM, BRYONIA (ALBA), EUPATORIUM PERFOLIATUM, GELSEMIUM SEMPERVIRENS, INFLUENZINUM, IPECACUANHA, KALI BICHROMICUM, NUX VOMICA, PHOSPHORUS, PHYTOLACCA DECANDRA openfda.generic_name manufacturer name Nenningers Naturals, LLC openfda.manufacturer_name ndc package 42731-083-01 openfda.package_ndc ndc product 42731-083 openfda.product_ndc ndc11 package 42731008301 derived:openfda.package_ndc spl id 104b8848-918c-4e72-b2cb-254539b50cec id spl set id 43bbed35-e351-409a-b6b6-7da1959634bf set_id unii 27YLU75U4W openfda.unii unii 11E6VI8VEG openfda.unii unii PS2DCE2WVF openfda.unii unii 269XH13919 openfda.unii unii F79059A38U openfda.unii unii 639KR60Q1Q openfda.unii unii AU5C98U4BB openfda.unii unii CYK5P89K8X openfda.unii unii 62I3C8233L openfda.unii unii T7J046YI2B openfda.unii unii RN2HC612GY openfda.unii unii U0NQ8555JD openfda.unii unii T4423S18FM openfda.unii unii 1W0775VX6E openfda.unii unii 6TU4EY6UNW 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 symptoms worsen or persist for more than 3 days consult a doctor. If pregnant or breast-feeding, 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.