Active Ingredient
Didecyl Dimethyl Ammonium Chloride 0.025%
Salicylic Acid 0.15%
NIACINAMIDE 0.5%
Milia Remover Treatment Liquid
FDA Label NDC 83818-001
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 Milia Remover Treatment (NDC 83818-001). 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
Fat grandule clearing Skin essence
Use
to fight and reduce signs of milia
Warnings
For external use only
Keep away from fire and flame
Do Not Use
if rash or irritation happens
When Using
Do not apply on other parts of the body
Avoid contact with eyes. In case of accidental contact, rinse eyes with a large amount of cool tap water
Stop Use
if rash or irritation happens
Ask Doctor
When Pregnant or breast-feeding
Keep Oot Of Reach Of Children
Keep Oot Of Reach Of Children
Directions
Slide the essence on the promatic area and use fingertips to massage until fully absorbed.
Other Information
Before use, read all information on the carton
Inactive Ingredients
DIMETHICONE,CYCLOPENTASILOXANE,PROPYLENE GLYCOL,HYDROXYACETOPHENONE,CYCLOHEXASILOXANE,ALLANTOIN
Questions
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