Active Ingredient
dimethylAmmoniumChloride 0.025%
Meoly Milia Remover 30 Ml Liquid
FDA Label NDC 83818-007
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Xinxin Yunhai Technology Co., Ltd. for the product Meoly Milia Remover 30 Ml (NDC 83818-007). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, do not use, when using, stop use, ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Disinfectant
Use
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.
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.
Ask Doctor
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
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