MILIA REMOVER TREATMENT- dideoyl dimethyl ammonium chloride liquid

MILIA REMOVER TREATMENT by

Drug Labeling and Warnings

MILIA REMOVER TREATMENT by is a Otc medication manufactured, distributed, or labeled by Hengyang Chuangjiujia Trading Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Dideoyl Dimethyl Ammonium Chloride 0.025%

PURPOSE

Disinfectant

INDICATIONS & USAGE

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

WARNINGS

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

DO NOT USE

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

WHEN USING

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

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

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

Glycerin
Salicylic acid
Xanthan gum
Ampelopsin
Tocopheryl Acetate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MILIA REMOVER TREATMENT 
dideoyl dimethyl ammonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84735-006
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 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
XANTHAN GUM (UNII: TTV12P4NEE)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
SALICYLIC ACID (UNII: O414PZ4LPZ)
DIHYDROMYRICETIN (UNII: KD8QND6427)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84735-006-01	1 in 1 BOX	04/01/2025
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/01/2025

Labeler - Hengyang Chuangjiujia Trading Co., Ltd. (977292157)

Establishment
Name	Address	ID/FEI	Business Operations
Hengyang Chuangjiujia Trading Co., Ltd.		977292157	manufacture(84735-006)