DERMFREE MILIA REMOVER
DERMFREE MILIA REMOVER is an FDA drug label for the active ingredient SALICYLIC ACID 1% MILIA REMOVER manufactured by Jiangxi Yudexi 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 20260723.
- Generic name
- SALICYLIC ACID 1% MILIA REMOVER
- Manufacturer
- Jiangxi Yudexi Pharmaceutical Co., LTD
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 85248-125
- Application
- M006
- Label effective
- 20260723
About this product
DERMFREE MILIA REMOVER is an FDA-registered drug product whose active ingredient is SALICYLIC ACID 1% MILIA REMOVER. It is labelled by Jiangxi Yudexi Pharmaceutical Co., LTD taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85248-125, application M006, label effective 20260723. It is one of 4 FDA drug label records sharing the active ingredient SALICYLIC ACID 1% MILIA REMOVER. 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 1% MILIA REMOVER are most often described in connection with: removal milia, skin bumps, aids exfoliating, cells helps. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Use For the removal of milia (skin bumps)Aids in exfoliating dead skin cells Helps smooth skin texture
Dosage & Administration
Directions L.Cleanse and dry the affected skin area thoroughly.2.Apply a thin layer of the product directly onto the milia (skin bumps) once or twice daily, as needed.3.Gently massage until fully absorbed.4.For best results, use consistently for 4 weeks.
Warnings
Warnings For external use only
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View labelHow products containing SALICYLIC ACID 1% MILIA REMOVER compare
FDA lists 4 drug label records with SALICYLIC ACID 1% MILIA REMOVER as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Jiangxi Yudexi Pharmaceutical Co., LTD | 4 |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is DERMFREE MILIA REMOVER used for?
Use For the removal of milia (skin bumps)Aids in exfoliating dead skin cells Helps smooth skin texture
Who makes DERMFREE MILIA REMOVER?
Jiangxi Yudexi Pharmaceutical Co., LTD is the labeler of record for DERMFREE MILIA REMOVER. 4 FDA label records share the active ingredient SALICYLIC ACID 1% MILIA REMOVER, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.
What form does DERMFREE 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 DERMFREE 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.
Are there other products containing SALICYLIC ACID 1% MILIA REMOVER?
Yes. 4 FDA drug label records list SALICYLIC ACID 1% MILIA REMOVER as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.
Has DERMFREE 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.