Winter Relief Flu and Fever

ACONITUM NAPELLUS 9C, ARNICA MONTANA 9C, BELLADONNA 9C, BRYONIA 9C, DULCAMARA 9C, EUCALYPTUS GLOBULUS 3C, EUPATORIUM PERFOLIATUM 9C BUCCAL HUMAN OTC DRUG

Winter Relief Flu and Fever is an FDA drug label for the active ingredient ACONITUM NAPELLUS 9C, ARNICA MONTANA 9C, BELLADONNA 9C, BRYONIA 9C, DULCAMARA 9C, EUCALYPTUS GLOBULUS 3C, EUPATORIUM PERFOLIATUM 9C manufactured by SEVENE USA administered by BUCCAL. 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 20260818.

Generic name
ACONITUM NAPELLUS 9C, ARNICA MONTANA 9C, BELLADONNA 9C, BRYONIA 9C, DULCAMARA 9C, EUCALYPTUS GLOBULUS 3C, EUPATORIUM PERFOLIATUM 9C
Manufacturer
SEVENE USA
Product type
HUMAN OTC DRUG
Route
BUCCAL
Dosage form
N/A
NDC
76472-7004
Application
N/A
Label effective
20260818

About this product

Winter Relief Flu and Fever is an FDA-registered drug product whose active ingredient is ACONITUM NAPELLUS 9C, ARNICA MONTANA 9C, BELLADONNA 9C, BRYONIA 9C, DULCAMARA 9C, EUCALYPTUS GLOBULUS 3C, EUPATORIUM PERFOLIATUM 9C. It is labelled by SEVENE USA taken by buccal and marketed as a human otc drug product. Identifiers on file: NDC 76472-7004, label effective 20260818. 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 9C, ARNICA MONTANA 9C, BELLADONNA 9C, BRYONIA 9C, DULCAMARA 9C, EUCALYPTUS GLOBULUS 3C, EUPATORIUM PERFOLIATUM 9C are most often described in connection with: sudden fever, aconitum napellus, cough associated, cold flu, arnica montana, trauma bruises, muscle pain, soreness stiffness. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

ACTIVE INGREDIENT Aconitum Napellus 9C - Arnica Montana 9C - Belladonna 9C - Bryonia 9C – Dulcamara 9C - Eucalyptus Globulus 3C – Eupatorium Perfoliatum 9C.

Indications & Usage

USE ACONITUM NAPELLUS Sudden Fever & Cough associated with Cold or Flu .* ARNICA MONTANA Trauma - Bruises - Muscle pain - Soreness - Stiffness - Swelling .* BELLADONNA Sudden Fever with Perspiration - Headache - Inflammation .* BRYONIA Muscle and Joint/Arthritis Pain Aggravated by Movement .* DULCAMARA Joint Pain triggered by Weather Change or Dampness .* EUCALYPTUS GLOBULUS Wet and Irritating cough - Congestion .* EUPATORIUM PERFOLIATUM Stiffness and Bone Pain associated with Fever Symptoms .*

Dosage & Administration

DIRECTIONS Adults/Children above 6 : spray 2 shots directly under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

Warnings

WARNINGS Consult a physician for use in children under 6 years of age. Contact a doctor if symptoms persist.

Frequently asked questions

What is Winter Relief Flu and Fever used for?
USE ACONITUM NAPELLUS Sudden Fever & Cough associated with Cold or Flu .* ARNICA MONTANA Trauma - Bruises - Muscle pain - Soreness - Stiffness - Swelling .* BELLADONNA Sudden Fever with Perspiration - Headache - Inflammation .* BRYONIA Muscle and Joint/Arthritis Pain Aggravated by Movement .* DULCAMARA Joint Pain triggered by Weather Change or Dampness .* EUCALYPTUS GLOBULUS Wet and Irritating …

Who makes Winter Relief Flu and Fever?
SEVENE USA is the labeler of record for Winter Relief Flu and Fever.

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

Is Winter Relief Flu and Fever 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 Winter Relief Flu and Fever 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.