MEOLY Milia Remover Serum

Manufacturer
Consilii LLC
Effective date
2023-08-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:27:12

Label at a glance#

ProductMEOLY Milia Remover Serum
Active ingredientDIDECYLDIMONIUM
Label structure12 sections

Dosage and administration

Apply daily after cleansing and toning. Twice a day for at least 4 weeks. Dispense a pea-size amount of the essence onto the problematic area and use fingertips to massage until fully absorbed. Keep using it for a period of time until the milia doesn’t appear again.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Didecyl dimethyl 0.025%

Purpose

OTC - PURPOSE SECTION

Disinfectant

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only. Stop using and ask a doctorif rash or irritation happens.

Do not use

OTC - DO NOT USE SECTION

on irritated skin on any area that is infected or reddened - Do not use it if pregnant or if there is any allergic reaction to this product - Avoid contact with eyes.

When Using

OTC - WHEN USING SECTION

For external use only Stop using and ask a doctorif rash or irritation happens.

Stop Use

OTC - STOP USE SECTION

Stop using and ask a doctorif rash or irritation happens. If contact with eyesoccurs, rinse thoroughly with water, Store in a coolshady place.

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product gets into eyes, flush with water for 15 minutes

If swallowed, get medical help or contact a Poison Control Center right away

Ask Doctor

OTC - ASK DOCTOR SECTION

Stop using and ask a doctorif rash or irritation happens.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply daily after cleansing and toning. Twice a day for at least 4 weeks.
Dispense a pea-size amount of the essence onto the problematic area and use fingertips to massage until fully absorbed.
Keep using it for a period of time until the milia doesn’t appear again.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, salicyle acid, dextrin,xanthan gum, amylopectin, tocopheryl acetate, dodecyl dimethyl benzyl ammonium chloride 0.025% ± 10%

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

0101

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83299-013-012024-01-30C16284748780-11030e365-1386-111a-e063-dadaa90a10e2031beb4d-610d-2a1b-e063-6394a90a553e

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83299-01383299-013-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
2763d6e8-e2bd-a406-e063-6394a90a6617031beb4d-610d-2a1b-e063-6394a90a553e2024-11-20WarningsExact identifier
spl set id: 031beb4d-610d-2a1b-e063-6394a90a553e

Reported adverse events (FAERS/openFDA)#

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