MILIA REMOVER TREATMENT- didecyl dimethyl ammonium chloride liquid 
Shenzhen Yangan Technology Co., Ltd.

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MILIA REMOVER TREATMENT

MILIA REMOVER TREATMENT

Didecyl dimethyl ammonium chloride 0.025%

Disinfectant

fight and reduce signs ofmilia, also help to resolveacne skin problems.

For external use only.

1. Cleanse your face with warm water. Dry the skin, and if possible use a facia moisturizer.
2. Drip the appropriate amount of milia remover on the milia spots and massage gently with your fingers.
3. Till the milia remover is completely absorbed, it is done and no need to remove it
4. To completely get rid of excessive skin oi and preventregrowth, Continue using for 4 weeks after the milia havebeen removed

Stop using and ask a doctor if rash or irritation happens.

2. Please keep it out of reach of infants and children.

1. Apply daily after cleansing and toning. Twice a day for at least 4 weeks.
2.Dispense a pea-size amount of the essence on to the probmatic area and usefingertips to massage until fuily absorbed.
3. Keep using it for a period of time until the milia doesn't appear again.

Store in a dry and cool place.

Water
Glycerin
Salicylic Acid
Dextrin
Xanthan Gum
Amylopectin
Tocopherol Acetate
Dodecyl Dimethyl Benzyl Ammonium Chloride 0.025% ± 10%

labellabel2

MILIA REMOVER TREATMENT 
didecyl dimethyl ammonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84023-701
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIDECYLDIMONIUM (UNII: Z7F472XQPA) (DIDECYLDIMONIUM - UNII:Z7F472XQPA) DIDECYLDIMONIUM0.025 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
AMYLOPECTIN (4,5-DIHYDROXY-1,3-DIMETHYLIMIDAZOLIDIN-2-ONE CROSS LINKED) (UNII: 48X4Z23U8J)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
BENZALKONIUM (UNII: 7N6JUD5X6Y)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
SALICYLIC ACID (UNII: O414PZ4LPZ)  
XANTHAN GUM (UNII: TTV12P4NEE)  
ICODEXTRIN (UNII: 2NX48Z0A9G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:84023-701-0120 mL in 1 BOTTLE; Type 0: Not a Combination Product03/22/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00603/22/2024
Labeler - Shenzhen Yangan Technology Co., Ltd. (419283765)
Establishment
NameAddressID/FEIBusiness Operations
Shenzhen Yangan Technology Co., Ltd.419283765manufacture(84023-701)

Revised: 3/2024
Document Id: 143ab751-5b70-75f1-e063-6394a90a1d1c
Set id: 143ab751-5b6f-75f1-e063-6394a90a1d1c
Version: 1
Effective Time: 20240322
 
Shenzhen Yangan Technology Co., Ltd.