Frankincense and Myrrh
Frankincense and Myrrh is an FDA drug label for the active ingredient INTENSIVE FOOT THERAPY LOTION manufactured by Wise Consumer Products Co. 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 20221227.
- Generic name
- INTENSIVE FOOT THERAPY LOTION
- Manufacturer
- Wise Consumer Products Co.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 42346-519
- Application
- N/A
- Label effective
- 20221227
About this product
Frankincense and Myrrh is an FDA-registered drug product whose active ingredient is INTENSIVE FOOT THERAPY LOTION. It is labelled by Wise Consumer Products Co. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 42346-519, label effective 20221227. 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 INTENSIVE FOOT THERAPY LOTION are most often described in connection with: temporary relief, minor aches. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses For the temporary relief of minor aches and pains.
Dosage & Administration
Directions Adults and children 12 years of age and older : apply to affected area not more than 3 to 4 times daily. Children under 12 years of age: consult a doctor.
Warnings
Warnings For external use only. Do not use on wounds or damaged skin over large areas of the body
Frequently asked questions
What is Frankincense and Myrrh used for?
Uses For the temporary relief of minor aches and pains.
Who makes Frankincense and Myrrh?
Wise Consumer Products Co. is the labeler of record for Frankincense and Myrrh.
What form does Frankincense and Myrrh 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 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 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.