Ultimate Topical Pain Relief Patch
Ultimate Topical Pain Relief Patch is an FDA drug label for the active ingredient CAPSAICIN AND MENTHOL, UNSPECIFIED FORM manufactured by Foshan Aqua Gel Biotech Co.,Ltd. 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 20171106.
- Generic name
- CAPSAICIN AND MENTHOL, UNSPECIFIED FORM
- Manufacturer
- Foshan Aqua Gel Biotech Co.,Ltd.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 69159-910
- Application
- part348
- Label effective
- 20171106
About this product
Ultimate Topical Pain Relief Patch is an FDA-registered drug product whose active ingredient is CAPSAICIN AND MENTHOL, UNSPECIFIED FORM. It is labelled by Foshan Aqua Gel Biotech Co.,Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 69159-910, application part348, label effective 20171106. 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 CAPSAICIN AND MENTHOL, UNSPECIFIED FORM are most often described in connection with: directions adults, apply affected, area change, patch times, daily children, years consult. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Directions Adults and children 12 and over apply to affected area; change patch 1 to 2 times daily Children under 12 years: Consult physician before use.
Dosage & Administration
Dosage and Administration Ultimate Topical Pain Relief Patch contains 0.0375% capsaicin and 5.00% menthol
Warnings
Warnings For external useonly. Avoid contact with eyes and mucous membranes. Do not use on wounds or damaged skin. Do not cover with bandage. Do not use if you are allergic to Menthol. Consult physician for use on children under 12. Stop use and ask a doctor if conditions worsen, if symptoms persist for more than 7 days or clear up and occur again with a few days, or if a rash, itching or excessive skin irritation occurs. If pregnant or breast feeding ask a health 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 Ultimate Topical Pain Relief Patch used for?
Directions Adults and children 12 and over apply to affected area; change patch 1 to 2 times daily Children under 12 years: Consult physician before use.
Who makes Ultimate Topical Pain Relief Patch?
Foshan Aqua Gel Biotech Co.,Ltd. is the labeler of record for Ultimate Topical Pain Relief Patch.
What form does Ultimate Topical Pain Relief Patch 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 Ultimate Topical Pain Relief Patch 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 Ultimate Topical Pain Relief Patch 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.