BYT BANGYTONG FOLLICULITIS
BYT BANGYTONG FOLLICULITIS is an FDA drug label for the active ingredient 5% BENZOYL PEROXIDE FOLLICULITIS manufactured by Shenzhen Jindali Technology 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 20260818.
- Generic name
- 5% BENZOYL PEROXIDE FOLLICULITIS
- Manufacturer
- Shenzhen Jindali Technology Co., Ltd
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 87382-026
- Application
- M005
- Label effective
- 20260818
About this product
BYT BANGYTONG FOLLICULITIS is an FDA-registered drug product whose active ingredient is 5% BENZOYL PEROXIDE FOLLICULITIS. It is labelled by Shenzhen Jindali Technology Co., Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87382-026, application M005, label effective 20260818. 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 5% BENZOYL PEROXIDE FOLLICULITIS are most often described in connection with: purpose topical. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Purpose Topical antibacterial
Dosage & Administration
Warnings For external use only.
Warnings
Do not use Do not use if you are sensitive to benzoyl peroxide.
Frequently asked questions
What is BYT BANGYTONG FOLLICULITIS used for?
Purpose Topical antibacterial
Who makes BYT BANGYTONG FOLLICULITIS?
Shenzhen Jindali Technology Co., Ltd is the labeler of record for BYT BANGYTONG FOLLICULITIS.
What form does BYT BANGYTONG FOLLICULITIS 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 BYT BANGYTONG FOLLICULITIS 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 BYT BANGYTONG FOLLICULITIS 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.