MILIA REMOVER TREATMENT

Manufacturer
Shenzhen Yangan Technology Co., Ltd.
Effective date
2024-03-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:10:11

Label at a glance#

ProductMILIA REMOVER TREATMENT
Active ingredientDIDECYLDIMONIUM
Label structure12 sections

Storage and handling

Store in a dry and cool place.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

MILIA REMOVER TREATMENT

OTC - ACTIVE INGREDIENT SECTION

Didecyl dimethyl ammonium chloride 0.025%

OTC - PURPOSE SECTION

Disinfectant

INDICATIONS & USAGE SECTION

fight and reduce signs ofmilia, also help to resolveacne skin problems.

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

1. Cleanse your face with warm water. Dry the skin, and if possible use a facia moisturizer.
2. Drip the appropriate amount of milia remover on the milia spots and massage gently with your fingers.
3. Till the milia remover is completely absorbed, it is done and no need to remove it
4. To completely get rid of excessive skin oi and preventregrowth, Continue using for 4 weeks after the milia havebeen removed

OTC - STOP USE SECTION

Stop using and ask a doctor if rash or irritation happens.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

2. Please keep it out of reach of infants and children.

DOSAGE & ADMINISTRATION SECTION

1. Apply daily after cleansing and toning. Twice a day for at least 4 weeks.
2.Dispense a pea-size amount of the essence on to the probmatic area and usefingertips to massage until fuily absorbed.
3. Keep using it for a period of time until the milia doesn't appear again.

STORAGE AND HANDLING SECTION

Store in a dry and cool place.

INACTIVE INGREDIENT SECTION

Water
Glycerin
Salicylic Acid
Dextrin
Xanthan Gum
Amylopectin
Tocopherol Acetate
Dodecyl Dimethyl Benzyl Ammonium Chloride 0.025% ± 10%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabellabel2label2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84023-701-01MILIA REMOVER TREATMENT20 mL in 1 BOTTLELIQUID201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84023-701MILIA REMOVER TREATMENT (DIDECYL DIMETHYL AMMONIUM CHLORIDE) LIQUID [SHENZHEN YANGAN TECHNOLOGY CO., LTD.]11 package rows20240323_143ab751-5b6f-75f1-e063-6394a90a1d1c.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84023-70184023-701-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
143ab751-5b70-75f1-e063-6394a90a1d1c143ab751-5b6f-75f1-e063-6394a90a1d1c2024-03-22WarningsExact identifier
spl id: 143ab751-5b70-75f1-e063-6394a90a1d1c
spl set id: 143ab751-5b6f-75f1-e063-6394a90a1d1c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.