GENTEAL TEARS MODERATE PRESERVATIVE FREE- dextran 70, hypromellose 2910 solution/ drops 
Alcon Laboratories, Inc.

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Drug Facts

Active IngredientsPurpose
Dextran 70 0.1%Lubricant
Hypromellose 2910 0.3%Lubricant

Uses

Warnings

For external use only

Do not use

When using this product

Stop use and ask a doctor if

you experience any of the following:

Keep out of reach of children.

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

Directions

Other information

Inactive ingredients

potassium chloride, purified water, sodium borate, sodium chloride. May contain hydrochloric acid and/or sodium hydroxide to adjust pH.

Questions?               

In the U.S. call 1 (800) 757-9195 (Mon-Fri 9AM-5PM CST)
alcon.medinfo@alcon.com

PRINCIPAL DISPLAY PANEL

PRESERVATIVE FREE

Moderate DRY EYE SYMPTOM RELIEF

GenTeal
® Tears

LUBRICANT EYE DROPS

LIQUID DROPS

Fast, Soothing Relief
Preservative Free Formula

Previously TEARS NATURALE® FREE LUBRICANT EYE DROPS

STERILE  36 Single-Use Vials 0.9 mL (0.03 FL OZ) Each

Alcon

GenTeal® Tears Lubricant Eye Drops
Preservative Free provide lasting relief
for moderate dry eye with the
convenience of a vial.

TAMPER EVIDENTY:
Do not use if vial is damaged or opened.

Distributed by:
Alcon Laboratories, Inc.,
6201 South Freeway
Fort Worth, Texas 76134

Country of Origin: France

435581

Carton Label
Carton Label
GENTEAL TEARS MODERATE PRESERVATIVE FREE 
dextran 70, hypromellose 2910 solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0065-8063
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)3 mg  in 1 mL
Dextran 70 (UNII: 7SA290YK68) (Dextran 70 - UNII:7SA290YK68) Dextran 701 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Potassium Chloride (UNII: 660YQ98I10)  
Water (UNII: 059QF0KO0R)  
Sodium Borate (UNII: 91MBZ8H3QO)  
Hydrochloric Acid (UNII: QTT17582CB)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Sodium Chloride (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0065-8063-0136 in 1 CARTON07/03/2018
1.9 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01807/03/2018
Labeler - Alcon Laboratories, Inc. (008018525)
Establishment
NameAddressID/FEIBusiness Operations
Kaysersberg Pharmaceuticals267486052manufacture(0065-8063)

Revised: 12/2023
Document Id: f7885429-659f-40b7-bbd7-d8680d1912f2
Set id: 37686e54-e64d-47c8-b082-b944a23cf6f1
Version: 8
Effective Time: 20231214
 
Alcon Laboratories, Inc.