Fat Granule Clearing Skin Essence

Manufacturer: Hengyang Chuangjiujia Trading Co., Ltd.
Effective date: 2025-05-21
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 01:01:22

Label at a glance#

ProductMILIA REMOVER TREATMENT

Active ingredientDIDECYLDIMONIUM

Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Dideoyl Dimethyl Ammonium Chloride 0.025%

OTC - PURPOSE SECTION

Disinfectant

INDICATIONS & USAGE SECTION

Uses: temporarily relieves these symptoms dueto hay fever or other upper respiratory allergies

WARNINGS SECTION

For extemal use only, Stop using and ask a doctorif rash or initation happens.

OTC - DO NOT USE SECTION

Do not use: In children less than 2years old. On open skin wounds.

OTC - WHEN USING SECTION

When Using: when using, keepout of eyes, ears ,mouth and anyopen hurt skin area.In case ofcontact with eyes, rinse eyesthoroughly with water.

OTC - STOP USE SECTION

Stop Use: Stop using and ask adoctor if irritation or rash occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. lf swallowed, get medical help orcontact the Poison Control Centerright away.

DOSAGE & ADMINISTRATION SECTION

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 INGREDIENT SECTION

Glycerin
Salicylic acid
Xanthan gum
Ampelopsin
Tocopheryl Acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
84735-006-01	MILIA REMOVER TREATMENT	1 in 1 BOX	LIQUID	1		4
84735-006-01	MILIA REMOVER TREATMENT	30 mL in 1 BOTTLE	LIQUID	30		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
84735-006	MILIA REMOVER TREATMENT (DIDEOYL DIMETHYL AMMONIUM CHLORIDE) LIQUID [HENGYANG CHUANGJIUJIA TRADING CO., LTD.]	4	2 package rows	20250523_31b27fa8-6f54-a265-e063-6394a90a19c3.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

MILIA REMOVER TREATMENT
Dideoyl Dimethyl Ammonium Chloride
GLYCERIN
XANTHAN GUM
.ALPHA.-TOCOPHEROL ACETATE
SALICYLIC ACID
DIDECYLDIMONIUM
DIHYDROMYRICETIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84735-006	84735-006-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
XANTHAN GUM	TTV12P4NEE	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
SALICYLIC ACID	O414PZ4LPZ	IACT
DIDECYLDIMONIUM	Z7F472XQPA	ACTIB
DIHYDROMYRICETIN	KD8QND6427	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
35a13839-b5ed-19ab-e063-6294a90a7115			31b27fa8-6f54-a265-e063-6394a90a19c3	2025-05-21	Warnings	Exact identifier spl id: 35a13839-b5ed-19ab-e063-6294a90a7115 spl set id: 31b27fa8-6f54-a265-e063-6394a90a19c3

Reported adverse events (FAERS/openFDA)#

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