EASYDERM BAND
EASYDERM BAND is an FDA drug label for the active ingredient PINE RESIN manufactured by Lydia 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 20230211.
- Generic name
- PINE RESIN
- Manufacturer
- Lydia Co., Ltd.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 72988-0037
- Application
- N/A
- Label effective
- 20230211
About this product
EASYDERM BAND is an FDA-registered drug product whose active ingredient is PINE RESIN. It is labelled by Lydia Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 72988-0037, label effective 20230211. 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 PINE RESIN are most often described in connection with: attach one, affected area, times day. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Attach one sheet to the affected area once to several times a day.
Dosage & Administration
for external use only
Warnings
■ Check the expiration date. ■ If you experience allergic reactions or infection symptoms such as rash, fever, or itching while using this product, stop using it immediately and receive appropriate treatment according to the doctor's instructions.
Frequently asked questions
What is EASYDERM BAND used for?
Attach one sheet to the affected area once to several times a day.
Who makes EASYDERM BAND?
Lydia Co., Ltd. is the labeler of record for EASYDERM BAND.
What form does EASYDERM BAND 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 EASYDERM BAND 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 EASYDERM BAND 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.