DRAVYNOR QUIT SMOKING Patches
DRAVYNOR QUIT SMOKING Patches is an FDA drug label for the active ingredient NICOTINE18% MENTHOL 0.3% QUIT SMOKING PATCHES manufactured by Wenzhou Yuyuan Pharmaceutical 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 20260724.
- Generic name
- NICOTINE18% MENTHOL 0.3% QUIT SMOKING PATCHES
- Manufacturer
- Wenzhou Yuyuan Pharmaceutical Co., Ltd.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 87786-028
- Application
- M017
- Label effective
- 20260724
About this product
DRAVYNOR QUIT SMOKING Patches is an FDA-registered drug product whose active ingredient is NICOTINE18% MENTHOL 0.3% QUIT SMOKING PATCHES. It is labelled by Wenzhou Yuyuan Pharmaceutical Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87786-028, application M017, label effective 20260724. 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 NICOTINE18% MENTHOL 0.3% QUIT SMOKING PATCHES are most often described in connection with: reduces withdrawal, symptoms including, nicotine craving, quitting smoking. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Use Use reduces withdrawal symptoms,including nicotine craving, associated with quitting smoking
Dosage & Administration
Directions If you are under 18 years of age, ask adoctor before use.Before using this product,need the enclosed self-help guide for complete directions and other information. Begin using the patch on your quit day.If you smoke more than 10 cigarettes per day, use the following schedule below. he used patch should be removed and a new one applied to a different skin site at the same time each day.If you have vivid dreams, you may removethe patch at bedtime and apply a new one in the morning.Do not wear more than one patch at a time.Do not cut patch in half or into smaller pieces.Do not leave patch on for more than 24 hours,because it may irritate your skin and loses strength after 24 hours.To avoid possible burns, remove patch before undergoing any MRl (magnetic resonance imaging)procedures.It is important to complete treatment,if you feel you need to use the patch for a longer period to keep from smoking, talk to your health care provider.Signs of excessive use may include nausea.vomiting,dizziness,weakness, or rapid heartbeat.lf these symptoms occur,remove the patch immediately and contact a doctor or poison control center
Warnings
Warnings If you are pregnant or breast-feeding, only use this medicine on the advice of your health care provider. Smoking can seriously harm your child. Try to stop smoking without using any nicotine replacement medicine, This medicine is believed to be safer than smoking.However, the risks to your child from this medicine are not fully known
Frequently asked questions
What is DRAVYNOR QUIT SMOKING Patches used for?
Use Use reduces withdrawal symptoms,including nicotine craving, associated with quitting smoking
Who makes DRAVYNOR QUIT SMOKING Patches?
Wenzhou Yuyuan Pharmaceutical Co., Ltd. is the labeler of record for DRAVYNOR QUIT SMOKING Patches.
What form does DRAVYNOR QUIT SMOKING Patches 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 DRAVYNOR QUIT SMOKING Patches 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 DRAVYNOR QUIT SMOKING Patches 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.