Frankincense and Myrrh Neuropathy

ACONITUM NAPELLUS, BRYONIA ALBA, HYPERICUM PERFORATUM TOPICAL HUMAN OTC DRUG

Frankincense and Myrrh Neuropathy is an FDA drug label for the active ingredient ACONITUM NAPELLUS, BRYONIA ALBA, HYPERICUM PERFORATUM manufactured by Wise Consumer Products administered by TOPICAL. 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 20211203.

Generic name
ACONITUM NAPELLUS, BRYONIA ALBA, HYPERICUM PERFORATUM
Manufacturer
Wise Consumer Products
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
42346-301
Application
N/A
Label effective
20211203

About this product

Frankincense and Myrrh Neuropathy is an FDA-registered drug product whose active ingredient is ACONITUM NAPELLUS, BRYONIA ALBA, HYPERICUM PERFORATUM. It is labelled by Wise Consumer Products taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 42346-301, label effective 20211203. 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, BRYONIA ALBA, HYPERICUM PERFORATUM are most often described in connection with: temporary relief, symptoms neuropathy, pain numbness, tingling weakness, homeopathic materia. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredients Aconitum napellus 3X HPUS Bryonia alba 3X HPUS Hypericum perforatum 3X HPUS The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

Indications & Usage

Uses: For temporary relief of the symptoms of neuropathy such as: pain numbness tingling weakness As per Homeopathic Materia Medica

Dosage & Administration

Directions: Adults and children 12 years of age and older: apply 10-30 drops into palm or hand and massage into feet or hands and affected areas massage oil in hand to coat painful areas can be used up to 4 times daily children under 12 years of age: consult a physician

Warnings

Warnings: For external use only. Do not apply to wounds, broken or damaged skin apply over large areas of the body When using this product avoid contact with eyes, mouth, nose or mucous membranes do not bandage tightly Stop use and ask a doctor if you are experiencing nerve pain in the feet and hands that includes burning, shooting, prickling/tingling pains, numbness or itching as these can be signs of diabetic neuropathy. See a healthcare professional regularly if you have or suspect you have these symptoms. condition worsens if symptoms persist for more than 7 days or clear up and occur again within a few days excessive skin irritation occurs If pregnant or breastfeeding , ask a health care professional before use. Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

Frequently asked questions

What is Frankincense and Myrrh Neuropathy used for?
Uses: For temporary relief of the symptoms of neuropathy such as: pain numbness tingling weakness As per Homeopathic Materia Medica

Who makes Frankincense and Myrrh Neuropathy?
Wise Consumer Products is the labeler of record for Frankincense and Myrrh Neuropathy.

What form does Frankincense and Myrrh Neuropathy come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Frankincense and Myrrh Neuropathy 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 Frankincense and Myrrh Neuropathy 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.