SUBIR EYELASH

Manufacturer: Dream Polymer
Effective date: 2021-03-30
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:39:20

Label at a glance#

ProductSUBIR EYELASH

Active ingredientButyl Acrylate

Label structure9 sections

Dosage and administration

• Apply Perm Glue to the silicone rod using brush • Pull lashes onto silicone rod and hold in place using lash lift tool • Remove adhesive with warm water after final processing

Storage and handling

・ Store in room temperature 0~30℃ ・ Avoid direct sunlight.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Butyl Acrylate 35%

Purpose

OTC - PURPOSE SECTION

Binding

Use

INDICATIONS & USAGE SECTION

Subir eyelash perm glue for eyelash Lifting

Warnings

WARNINGS SECTION

• Be careful not to get in your eyes. • Keep out of reach of children.
• If it gets into your eyes, immediately wash it off with clean water several times.
• Wear appropriate gloves during the procedure.
• Do not eat. • Store in a cool place away from direct sunlight.
• Follow the recommendations.
• After use, if skin irritation such as rash or itching persists, stop use and consult a doctor or pharmacist

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

 Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply Perm Glue to the silicone rod using brush
• Pull lashes onto silicone rod and hold in place using lash lift tool
• Remove adhesive with warm water after final processing

Other information

STORAGE AND HANDLING SECTION

・ Store in room temperature 0~30℃
・ Avoid direct sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Propylene Glycol, Dextrin, Polyvinyl Pyrrolidone, Biotin

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
81716-005-01	2022-07-29	C162847	48780-1	e4f33bdf-9dad-d8a0-e053-dadaa90a6e4e	ea886530-0c2a-411c-8af7-b6c6bb6d41e1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
81716-005-01	SUBIR EYELASH	10 g in 1 TUBE	CREAM	10		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81716-005	SUBIR EYELASH (PERM GLUE) CREAM [DREAM POLYMER]	1	Legacy NDC, 1 package rows	20210331_ea886530-0c2a-411c-8af7-b6c6bb6d41e1.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

SUBIR EYELASH
PERM GLUE
Butyl Acrylate
Water
Propylene Glycol
Biotin

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81716-005	81716-005-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Butyl Acrylate	705NM8U35V	ACTIB
Water	059QF0KO0R	IACT
Propylene Glycol	6DC9Q167V3	IACT
Biotin	6SO6U10H04	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
09cf74e7-b637-40e4-9137-d80009b2828a			ea886530-0c2a-411c-8af7-b6c6bb6d41e1	2021-03-30	Warnings	Exact identifier spl id: 09cf74e7-b637-40e4-9137-d80009b2828a spl set id: ea886530-0c2a-411c-8af7-b6c6bb6d41e1

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.