Quick answers
- What is Didecyldimonium chloride used for?
- The Drug Facts label of Lepnuns MILIA REMOVER (Jiangxi Yudexi Pharmaceutical Co., Ltd) lists these uses: temporarily relieves these symptoms due to hay fever or other upper respiratory allergies..
- Do I need a prescription for Didecyldimonium chloride?
- No. The products on this page are sold without a prescription (over the counter).
- Is a store brand the same as the name brand?
- Products listed together below have the same active ingredient, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
- Has Didecyldimonium chloride been recalled?
- No recall linked to these products appears in the FDA enforcement reports we use.
Drug Facts label
Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.
Lepnuns MILIA REMOVER · Jiangxi Yudexi Pharmaceutical Co., Ltd
Didecyldimonium chloride 0.25%, liquid (topical)
Active ingredient
Didecyl dimethyl Ammonium Chloride 0.025%士10%
Purpose
Disinfectant
Uses
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies.
Warnings
For external use only, Stop using and ask a doctor,if rash or irritation happens.
Do not use
In children less than 2 years old. On open skin wounds. Ask Doctor Stop using and ask a doctor if ir irritation or rash occurs. When Using When using, keep out of eyes, ears ,mouth and any open hurt skin area.in case of contact with eyes, rinse eyes thoroughly with water. Stop Use Stop using and ask a doctor if ir irritation or rash occurs. Keep Oot Of Reach Of Children
Keep out of reach of children
lf swallowed, get medical help or contact the Poison Control Center right away.
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.
Inactive ingredients
Glycerin, Salicylic acid, dextrin,xanthan gum,amylopectin, tocopheryl acetate.
— FDA label of Lepnuns MILIA REMOVER, Jiangxi Yudexi Pharmaceutical Co., Ltd, effective July 20, 2026. See the official label on DailyMed →
MEOLY Milia Remover 30 ml · Shenzhen Xinxin Yunhai Technology Co., Ltd.
Didecyldimonium chloride 0.025%, liquid (topical)
Active ingredient
dimethylAmmoniumChloride 0.025%
Purpose
Disinfectant
Uses
temporarily relieves these symptoms dueto hay fever or other upper respiratory allergies
Warnings
For external use only, Stop using and ask a doctorif rash or irritation happens.
Do not use
In children less thanyears old. On open skin wounds. Ask Doctor Stop using and ask adoctor if irritation or rash occurs. When Using When using, keepout of eyes,ears ,mouth and anyopen hurt skin area. In case ofcontact with eyes, rinse eyesthoroughly with water. Stop Use Stop using and ask adoctor if irritation or rash occurs. Keep Oot Of Reach Of Children
Keep out of reach of children
lfswallowed, get medical help orcontact the Poison Control Centerright away.
Directions
1. Apply daily after cleansing and toning. Twice aday for at least 4 weeks.2.Dispense a pea-size amount of the essence ontothe problematic area and use fingertips to massageuntil fully absorbed.3.Keep using it for a period of time until the miliadoesn't appear again
Inactive ingredients
Glycerin, salicyle acid, dextrin,xanthan gum,amylopectin, tocopheryl acetate, dodecyl dimethybenzyl ammonium chloride
— FDA label of MEOLY Milia Remover 30 ml, Shenzhen Xinxin Yunhai Technology Co., Ltd., effective November 25, 2024. See the official label on DailyMed →
This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.
Same medicine, other brands
Each group lists the products that have exactly the same active ingredient, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.
Didecyldimonium chloride 0.25% · liquid (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Lepnuns MILIA REMOVER | Jiangxi Yudexi Pharmaceutical Co., Ltd | DailyMed |
Didecyldimonium chloride 0.025% · liquid (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| MEOLY Milia Remover 30 ml | Shenzhen Xinxin Yunhai Technology Co., Ltd. | DailyMed |
Companies that sell this medicine
The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.
- Jiangxi Yudexi Pharmaceutical Co., Ltd1 product
- Shenzhen Xinxin Yunhai Technology Co., Ltd.1 product
Recalls
No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- FDA rule for the Drug Facts label (21 CFR 201.66)
Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.