Lepnuns MILIA REMOVER
Lepnuns MILIA REMOVER is an FDA drug label for the active ingredient DIDECYL DIMETHYL AMMONIUM CHLORIDE 0.025% 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 20260720.
- Generic name
- DIDECYL DIMETHYL AMMONIUM CHLORIDE 0.025% MILIA REMOVER
- Manufacturer
- Jiangxi Yudexi Pharmaceutical Co., LTD
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 85248-020
- Application
- M006
- Label effective
- 20260720
About this product
Lepnuns MILIA REMOVER is an FDA-registered drug product whose active ingredient is DIDECYL DIMETHYL AMMONIUM CHLORIDE 0.025% 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 85248-020, application M006, label effective 20260720. 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 DIDECYL DIMETHYL AMMONIUM CHLORIDE 0.025% MILIA REMOVER are most often described in connection with: temporarily relieves, symptoms due, hay fever, upper respiratory. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Use temporarily relieves these symptoms due to hay fever or other upper respiratory allergies.
Dosage & Administration
Directions 1. Apply daily after cleansing and toning.Twice a day for at least 4 weeks. 2.Dispense a pea-size amount of the essence onto the problematic area and use fingertips to massage until fully absorbed. 3,Keep using it for a period of time until the milia doesn't appear again.
Warnings
Warnings For external use only, Stop using and ask a doctor,if rash or irritation happens.
Frequently asked questions
What is Lepnuns MILIA REMOVER used for?
Use temporarily relieves these symptoms due to hay fever or other upper respiratory allergies.
Who makes Lepnuns MILIA REMOVER?
Jiangxi Yudexi Pharmaceutical Co., LTD is the labeler of record for Lepnuns MILIA REMOVER.
What form does Lepnuns 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 Lepnuns 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 Lepnuns 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.