ISOPTO TEARS- hypromellose 2910 solution 
Alcon Laboratories, Inc.

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Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Hypromellose 2910 0.5%

OTC - PURPOSE SECTION

Lubricant

INDICATIONS & USAGE SECTION

Uses

WARNINGS SECTION

For external use only
Do not use

OTC - WHEN USING SECTION

When using this product

OTC - STOP USE SECTION

Stop use and ask a doctor if

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

OTHER INFORMATION

INACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.01% as preservative, dibasic sodium phosphate, monobasic sodium phosphate, purified water, sodium chloride, sodium citrate.

OTC - QUESTIONS SECTION

In the U.S. call 1-800-757-9195

PRINCIPAL DISPLAY PANEL

Alcon®

Isopto® Tears
LUBRICANT
Eye Drops
Hypromellose (Ophthalmic Solution)

For Relief of Dry Eyes

STERILE
15 mL (1/2 FL OZ)

TAMPER EVIDENT: For your protection, this bottle has an imprinted seal around the neck. Do not use if seal is damaged or missing at time of purchase.

Alcon®

ALCON LABORATORIES, INC.
Fort Worth, Texas 76134 USA

World's largest manufacturer of ophthalmic preparations


©2000, 2010 Alcon, Inc.
Printed in USA


9001579-0410

Carton
ISOPTO TEARS 
hypromellose 2910 solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0998-0408
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Hypromellose 2910 (4000 Mpa.s) (UNII: RN3152OP35) (Hypromellose 2910 (4000 Mpa.s) - UNII:RN3152OP35) Hypromellose 2910 (4000 Mpa.s)5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Benzalkonium Chloride (UNII: F5UM2KM3W7)  
Sodium Phosphate, Dibasic (UNII: GR686LBA74)  
Sodium Phosphate, Monobasic (UNII: 3980JIH2SW)  
Water (UNII: 059QF0KO0R)  
Sodium Chloride (UNII: 451W47IQ8X)  
Sodium Citrate (UNII: 1Q73Q2JULR)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0998-0408-1515 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product09/30/199012/31/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01809/30/199012/31/2024
Labeler - Alcon Laboratories, Inc. (008018525)
Registrant - Alcon Laboratories, Inc. (008018525)
Establishment
NameAddressID/FEIBusiness Operations
Alcon Research Ltd007672236MANUFACTURE(0998-0408)

Revised: 12/2023
Document Id: 087ce08b-8271-4eda-9ac0-3554dbe54dd1
Set id: f1753a5b-7ba8-103d-6fe4-d93a3fc5f803
Version: 7
Effective Time: 20231214
 
Alcon Laboratories, Inc.