Flu Fix

ACONITUM NAPELLUS, ALLIUM CEPA, ANIS BARBARIAE, BRYONIA ALBA, ECHINACEA ANGUSTIFOLIA, EUPATORIUM PERFOLLATUM, GELSEMIUM SEMPERVIRENS, IPECACAUANHA, NUX VOMICA, PULSATILLA, RHUS TOXICODENDRON ORAL HUMAN OTC DRUG

Flu Fix is an FDA drug label for the active ingredient ACONITUM NAPELLUS, ALLIUM CEPA, ANIS BARBARIAE, BRYONIA ALBA, ECHINACEA ANGUSTIFOLIA, EUPATORIUM PERFOLLATUM, GELSEMIUM SEMPERVIRENS, IPECACAUANHA, NUX VOMICA, PULSATILLA, RHUS TOXICODENDRON manufactured by Genexa Inc. administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260829.

Generic name
ACONITUM NAPELLUS, ALLIUM CEPA, ANIS BARBARIAE, BRYONIA ALBA, ECHINACEA ANGUSTIFOLIA, EUPATORIUM PERFOLLATUM, GELSEMIUM SEMPERVIRENS, IPECACAUANHA, NUX VOMICA, PULSATILLA, RHUS TOXICODENDRON
Manufacturer
Genexa Inc.
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
69676-0010
Application
N/A
Label effective
20260829

About this product

Flu Fix is an FDA-registered drug product whose active ingredient is ACONITUM NAPELLUS, ALLIUM CEPA, ANIS BARBARIAE, BRYONIA ALBA, ECHINACEA ANGUSTIFOLIA, EUPATORIUM PERFOLLATUM, GELSEMIUM SEMPERVIRENS, IPECACAUANHA, NUX VOMICA, PULSATILLA, RHUS TOXICODENDRON. It is labelled by Genexa Inc. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 69676-0010, label effective 20260829. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing ACONITUM NAPELLUS, ALLIUM CEPA, ANIS BARBARIAE, BRYONIA ALBA, ECHINACEA ANGUSTIFOLIA, EUPATORIUM PERFOLLATUM, GELSEMIUM SEMPERVIRENS, IPECACAUANHA, NUX VOMICA, PULSATILLA, RHUS TOXICODENDRON are most often described in connection with: addresses symptoms, body aches, headache chills, fatigue congestion, sore throat. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredients** Aconitum napellus 12X HPUS Allium cepa 6X HPUS Anas barbariae 6C HPUS Bryonia alba 9X HPUS Echinacea angustifolia 6X HPUS Eupatorium perfoliatum 6X HPUS Euphrasia officinalis 6X HPUS Gelsemium sempervirens 12X HPUS Ipecacuanha 12X HPUS Nux vomica 12X HPUS Pulsatilla 9X HPUS Rhus toxicodendron 12X HPUS "HPUS" indicates that this ingredient is officially included in the Homeopathic Pharmacopoeia of the United States.

Indications & Usage

Uses* addresses symptoms associated with the flu, such as: body aches headache chills fatigue congestion sore throat

Dosage & Administration

Directions take dose at the onset of symptoms chew tablets before swallowing; do not swallow whole repeat dose every 4-6 hours as needed adults and children 12 years of age & older 2 tablets children 4-11 years of age 1 tablet children under 4 years of age ask a doctor before use

Warnings

Warnings Stop use and ask a doctor if difficulty breathing, vomiting, skin rash, diarrhea or fever above 100°F (38°C) develops symptoms persist for more than 2 days or worsen. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children.

Frequently asked questions

What is Flu Fix used for?
Uses* addresses symptoms associated with the flu, such as: body aches headache chills fatigue congestion sore throat

Who makes Flu Fix?
Genexa Inc. is the labeler of record for Flu Fix.

What form does Flu Fix come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Flu Fix prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has Flu Fix been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.