Milia Remover Serum

Manufacturer
Consilii LLC
Effective date
2023-04-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:33:17

Label at a glance#

ProductMilia Remover Serum
Active ingredientAMMONIUM CATION, AMYLOPECTIN (4,5-DIHYDROXY-1,3-DIMETHYLIMIDAZOLIDIN-2-ONE CROSS LINKED)
Label structure12 sections

Dosage and administration

Apply gently to skin

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

amylopectin 1%.

ammonium 0.8%

Purpose

OTC - PURPOSE SECTION

Disinfectant

Use

INDICATIONS & USAGE SECTION

fight and reduce signs of milia, alsohelp to resolve acne skin problems.

Warnings

WARNINGS SECTION

For external use only. Stop using and ask adoctor if rash or irritation happens

Do not use

OTC - DO NOT USE SECTION

On broken skin
On eyes area

WHEN USING

OTC - WHEN USING SECTION

For external use only.
Avoid contacting with eyes, flush with water immediately if it gets into eyes.
Children should use it under the supervision of adults.
Keep out of reach of children.

STOP USE section

OTC - STOP USE SECTION

lf contact with eyesoccurs, rinse thoroughly with water.Store in a cool, dark place.

ASK DOCTOR

OTC - ASK DOCTOR SECTION

Stop using and ask a doctoif rash or irritation happens.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply gently to skin

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerol

salicylic acid

Dextrin

xanthan gum

amylopectin

tocopherol acetate

dodecyl dimethybenzyl ammonium

water

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

59855985

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83299-003-012024-01-30C16284748780-11030e365-48c8-111a-e063-dadaa90a10e283299-003 Milia Remover Serum

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83299-00383299-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
20d140c3-79c9-c910-e063-6394a90aa571f8bac722-88e4-7431-e053-6294a90ac1302024-08-29WarningsExact identifier
spl set id: f8bac722-88e4-7431-e053-6294a90ac130

Reported adverse events (FAERS/openFDA)#

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