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 23:39:19

Label at a glance#

ProductSUBIR EYELASH

Active ingredient2-OCTYL CYANOACRYLATE

Label structure9 sections

Dosage and administration

・ Shake the glue bottle. ・ Do not let the glue nozzle make contact to the surface. ・ 'Burp' the glue bottle. ・ Wipe the glue nozzle with a lint-free paper. ・ Close the lid tightly in between uses.

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

n-BUTYL CYANOACRYLATE 91.5%

Purpose

OTC - PURPOSE SECTION

Purpose:Adhesion

Use

INDICATIONS & USAGE SECTION

Subir eyelash extension glue for eyelash extension

Warnings

WARNINGS SECTION

・ Be careful not to get in your eyes.
・ If it gets into your eyes, immediately wash it off with clean water
several times.
・ Wear appropriate gloves during the procedure.
・Do not eat. ・ Keep out of reach of children.
・ Store in a cool place away from direct sunlight.
・ For professional use only. ・ 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

・ Shake the glue bottle.
・ Do not let the glue nozzle make contact to the surface.
・ 'Burp' the glue bottle.
・ Wipe the glue nozzle with a lint-free paper.
・ Close the lid tightly in between uses.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

POLYMETHYLMETHACRYLATE, Diisononyl adipate, Carbon black

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
81716-001-01	2022-07-29	C162847	48780-1	e4f33bdf-af6f-d8a0-e053-dadaa90a6e4e	d78ace98-2448-4000-a1c6-8b3abd0ba272

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
81716-001-01	SUBIR EYELASH	10 g in 1 BOTTLE	CREAM	10		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81716-001	SUBIR EYELASH (EXTENSION GLUE) CREAM [DREAM POLYMER]	1	Legacy NDC, 1 package rows	20210331_d78ace98-2448-4000-a1c6-8b3abd0ba272.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

SUBIR EYELASH
Extension Glue
2-OCTYL CYANOACRYLATE
Diisononyl adipate

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81716-001	81716-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
2-OCTYL CYANOACRYLATE	L23GHX71SK	ACTIB
Diisononyl adipate	BMQ5JF4857	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
c9f50ea3-da50-47e1-8234-ec59fad7a33b			d78ace98-2448-4000-a1c6-8b3abd0ba272	2021-03-30	Warnings	Exact identifier spl id: c9f50ea3-da50-47e1-8234-ec59fad7a33b spl set id: d78ace98-2448-4000-a1c6-8b3abd0ba272

Reported adverse events (FAERS/openFDA)#

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