MILIA REMOVER TREATMENT- milia remover liquid

Milia Remover Treatment by

Drug Labeling and Warnings

Milia Remover Treatment by is a Otc medication manufactured, distributed, or labeled by Shenzhen Xinxin Yunhai Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Didecyl Dimethyl Ammonium Chloride 0.025%

Salicylic Acid 0.15%

NIACINAMIDE 0.5%

Purpose

Fat grandule clearing Skin essence

Use

to fight and reduce signs of milia

Warnings

For external use only

Keep away from fire and flame

Do not use

if rash or irritation happens

When Using

Do not apply on other parts of the body

Avoid contact with eyes. In case of accidental contact, rinse eyes with a large amount of cool tap water

Stop Use

if rash or irritation happens

Ask Doctor

When Pregnant or breast-feeding

Keep Oot Of Reach Of Children

Keep Oot Of Reach Of Children

Directions

Slide the essence on the promatic area and use fingertips to massage until fully absorbed.

Other information

Before use, read all information on the carton

Inactive ingredients

DIMETHICONE,CYCLOPENTASILOXANE,PROPYLENE GLYCOL,HYDROXYACETOPHENONE,CYCLOHEXASILOXANE,ALLANTOIN

Questions

novensabeauty@gmail.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MILIA REMOVER TREATMENT 
milia remover liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83818-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.15 g  in 100 mL
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) (DIDECYLDIMONIUM - UNII:Z7F472XQPA)	DIDECYLDIMONIUM CHLORIDE	0.025 g  in 100 mL
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	0.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
DIMETHICONE (UNII: 92RU3N3Y1O)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
ALLANTOIN (UNII: 344S277G0Z)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83818-001-01	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/19/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	11/19/2023

Labeler - Shenzhen Xinxin Yunhai Technology Co., Ltd. (699816806)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Xinxin Yunhai Technology Co., Ltd.		699816806	manufacture(83818-001) , label(83818-001)