MEOLY MILIA REMOVER SERUM- milia remover serum liquid

MEOLY Milia Remover Serum by

Drug Labeling and Warnings

MEOLY Milia Remover Serum by is a Otc medication manufactured, distributed, or labeled by Consilii LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Didecyl dimethyl 0.025%

Purpose

Disinfectant

Use

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

Warnings

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

Do not use

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

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

Stop Use

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

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

Stop using and ask a doctorif rash or irritation happens.

Directions

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

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

PACKAGE LABEL

INGREDIENTS AND APPEARANCE

MEOLY MILIA REMOVER SERUM 
milia remover serum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83299-013
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIDECYLDIMONIUM (UNII: Z7F472XQPA) (DIDECYLDIMONIUM - UNII:Z7F472XQPA)	DIDECYLDIMONIUM	0.025 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
AMYLOPECTIN, CORN (UNII: TQI9LJM246)
GLYCERIN (UNII: PDC6A3C0OX)
SALICYLIC ACID (UNII: O414PZ4LPZ)
XANTHAN GUM (UNII: TTV12P4NEE)
ICODEXTRIN (UNII: 2NX48Z0A9G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83299-013-01	30 g in 1 BOTTLE; Type 0: Not a Combination Product	08/14/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	M005	08/14/2023

Labeler - Consilii LLC (118891890)

Establishment
Name	Address	ID/FEI	Business Operations
Consilii LLC		118891890	manufacture(83299-013) , label(83299-013)