Milia Remover Treatment

Manufacturer: Shenzhen Xinxin Yunhai Technology Co., Ltd.
Effective date: 2025-01-04
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 00:50:36

Label at a glance#

ProductMilia Remover Treatment

Active ingredientSALICYLIC ACID, DIDECYLDIMONIUM CHLORIDE, NIACINAMIDE

Label structure14 sections

Dosage and administration

Slide the essence on the promatic area and use fingertips to massage until fully absorbed.

Storage and handling

Before use, read all information on the carton

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Didecyl Dimethyl Ammonium Chloride 0.025%

Salicylic Acid 0.15%

NIACINAMIDE 0.5%

Purpose

OTC - PURPOSE SECTION

Fat grandule clearing Skin essence

Use

INDICATIONS & USAGE SECTION

to fight and reduce signs of milia

Warnings

WARNINGS SECTION

For external use only

Keep away from fire and flame

Do not use

OTC - DO NOT USE SECTION

if rash or irritation happens

When Using

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

if rash or irritation happens

Ask Doctor

OTC - ASK DOCTOR SECTION

When Pregnant or breast-feeding

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Oot Of Reach Of Children

Directions

DOSAGE & ADMINISTRATION SECTION

Slide the essence on the promatic area and use fingertips to massage until fully absorbed.

Other information

STORAGE AND HANDLING SECTION

Before use, read all information on the carton

Inactive ingredients

INACTIVE INGREDIENT SECTION

DIMETHICONE,CYCLOPENTASILOXANE,PROPYLENE GLYCOL,HYDROXYACETOPHENONE,CYCLOHEXASILOXANE,ALLANTOIN

Questions

OTC - QUESTIONS SECTION

novensabeauty@gmail.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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
83818-001-01	Milia Remover Treatment	15 mL in 1 BOTTLE	LIQUID	15		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
83818-001	MILIA REMOVER TREATMENT (MILIA REMOVER) LIQUID [SHENZHEN XINXIN YUNHAI TECHNOLOGY CO., LTD.]	2	Current NDC, 1 package rows	20250105_0a8c7bdb-19f4-54c9-e063-6394a90ac5f5.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

Milia Remover Treatment
Milia Remover
SALICYLIC ACID
DIDECYLDIMONIUM CHLORIDE
DIDECYLDIMONIUM
DIMETHICONE
NIACINAMIDE
CYCLOMETHICONE 5
PROPYLENE GLYCOL
CYCLOMETHICONE 6
ALLANTOIN
HYDROXYACETOPHENONE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
83818-001	83818-001-01

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
SALICYLIC ACID	O414PZ4LPZ	ACTIB
DIDECYLDIMONIUM CHLORIDE	JXN40O9Y9B	ACTIB
DIMETHICONE	92RU3N3Y1O	IACT
NIACINAMIDE	25X51I8RD4	ACTIB
CYCLOMETHICONE 5	0THT5PCI0R	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
CYCLOMETHICONE 6	XHK3U310BA	IACT
ALLANTOIN	344S277G0Z	IACT
HYDROXYACETOPHENONE	G1L3HT4CMH	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
Milia Remover Treatment	MILIA REMOVER	Shenzhen Xinxin Yunhai Technology Co., Ltd.	0a8c7bdb-19f4-54c9-e063-6394a90ac5f5	2025-01-04	Warnings	Exact identifier ndc (package): 83818-001-01 ndc (product): 83818-001 ndc11 (package): 83818000101 spl id: 2adc1db8-796a-7778-e063-6294a90a69fb spl set id: 0a8c7bdb-19f4-54c9-e063-6394a90ac5f5

Reported adverse events (FAERS/openFDA)#

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