BUTTERFLYS TEAR MILIA REMOVER- salicylic acid 1% milia remover liquid

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredient

salicylic acid 1%

Purpose

Skin Papule
Refining Solution

Use

Aids in smoothing skin texture through gentle exfoliation.

Warnings

·For external use only.
·Keep away from heat or flame.

Do not use

In children less than 2 years old.
On open skin wounds.

When Using

·When using, keep out of eyes, ears, mouth and any open broken skin area.
·In case of contact with eyes, rinse eyes thoroughly with water.

Stop Use

·Stop using and ask a doctor if rash or irritation happens.
·If contact with eyes occurs, rinse thoroughly with water.

Ask Doctor

·Stop using and ask a doctor if rash or irritation happens.
·If contact with eyes occurs, rinse thoroughly with water.

Keep Out Of Reach Of Children

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

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 your fingertips to massage until it is fully absorbed.
·Keep using it for a period of time until the skin papule doesn't appear again.

Other information

Store between 20° to 25°C (68° to 77°F) and keep tightly closed.

Inactive ingredients

Water,Glycerin, Dextrin,Xanthan Gum,Amylopectin, Tocopheryl Acetate.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BUTTERFLYS TEAR MILIA REMOVER 
salicylic acid 1% milia remover liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85248-213
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
XANTHAN GUM (UNII: TTV12P4NEE)
AMYLOPECTIN, CORN (UNII: TQI9LJM246)
DEXTRIN, CORN (UNII: VAD2K35XAJ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85248-213-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/19/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	05/19/2026

Labeler - Jiangxi Yudexi Pharmaceutical Co., LTD (455662836)