BYT BANGYTONG MILIA REMOVER
BYT BANGYTONG MILIA REMOVER is an FDA drug label for the active ingredient SALICYLIC ACID 2% MILIA REMOVER 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 20260819.
- Generic name
- SALICYLIC ACID 2% MILIA REMOVER
- Manufacturer
- Shenzhen Jindali Technology Co., Ltd
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 87382-027
- Application
- M006
- Label effective
- 20260819
About this product
BYT BANGYTONG MILIA REMOVER is an FDA-registered drug product whose active ingredient is SALICYLIC ACID 2% MILIA REMOVER. It is labelled by Shenzhen Jindali Technology Co., Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87382-027, application M006, label effective 20260819. 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 SALICYLIC ACID 2% MILIA REMOVER are most often described in connection with: purpose milia. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Purpose Milia Remover
Dosage & Administration
Warnings For external use only.
Warnings
Do not use condition worsens or does not improve within 4 weeks,Severe redness, burning, or swelling occurs. If pregnant or breast-feeding, ask a health professional before use.
Frequently asked questions
What is BYT BANGYTONG MILIA REMOVER used for?
Purpose Milia Remover
Who makes BYT BANGYTONG MILIA REMOVER?
Shenzhen Jindali Technology Co., Ltd is the labeler of record for BYT BANGYTONG MILIA REMOVER.
What form does BYT BANGYTONG MILIA REMOVER 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 MILIA REMOVER 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 MILIA REMOVER 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.