Endura

Manufacturer: Allergan, Inc.
Effective date: 2019-11-26
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-05-31 21:16:23

Label at a glance#

ProductEndura

Active ingredientGLYCERIN, POLYSORBATE 80

Label structure1 sections

Label contents#

Full prescribing information#

Principal Display Panel - Carton Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRESERVATIVE-FREE
FOR SENSITIVE EYES
Endura^®
Lubricant Eye Drops
Long Lasting Relief
for Symptoms of Dry Eye
Allergan_TM
30 Sterile Single-Use Containers
0.4 mL each

PRESERVATIVE-FREE FOR SENSITIVE EYES Endura® Lubricant Eye Drops Long Lasting Relief for Symptoms of Dry Eye AllerganTM 30 Sterile Single-Use Containers 0.4 mL each

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
359595	glycerin 1 % / polysorbate 80 1 % Ophthalmic Solution	PSN	5
359595	glycerin 10 MG/ML / polysorbate 80 10 MG/ML Ophthalmic Solution	SCD	5
359595	glycerin 1 % / polysorbate 80 1 % Ophthalmic Solution	SY	5

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
GLYCERIN Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0023-9235-20	Endura	30 in 1 CARTON	SOLUTION/ DROPS	30		5
0023-9235-20	Endura	0.4 mL in 1 CONTAINER	SOLUTION/ DROPS	0.4		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0023-9235	ENDURA (GLYCERIN AND POLYSORBATE 80) SOLUTION/ DROPS [ALLERGAN, INC.]	5	2 package rows	20241105_bbbbab91-5f9d-42d5-87fc-d629da20e8b1.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

Endura
Glycerin and Polysorbate 80
GLYCERIN
POLYSORBATE 80
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)
CASTOR OIL
MANNITOL
WATER
SODIUM HYDROXIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0023-9235	0023-9235-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	ACTIB
POLYSORBATE 80	6OZP39ZG8H	ACTIB
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)	71DD5V995L	IACT
CASTOR OIL	D5340Y2I9G	IACT
MANNITOL	3OWL53L36A	IACT
WATER	059QF0KO0R	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT

Source Document#

Source XML · Source PDF

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
5fab8f60-8534-4a2f-97e9-de497775092e			bbbbab91-5f9d-42d5-87fc-d629da20e8b1	2019-11-26		Exact identifier spl id: 5fab8f60-8534-4a2f-97e9-de497775092e spl set id: bbbbab91-5f9d-42d5-87fc-d629da20e8b1

Reported adverse events (FAERS/openFDA)#

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