ALCON TEARS LUBRICANT EYE DROPS- hypromellose 2910 solution/ drops 
Alcon Laboratories, Inc.

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Drug Facts

Active ingredientsPurpose
Hypromellose 2910 0.5%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

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

Questions?

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

PRINCIPAL DISPLAY PANEL

Alcon Tears

LUBRICANT
Eye Drops

For Relief of Dry Eye Symptoms

STERILE


15 mL (1/2 FL OZ)

Alcon

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

Printed in USA

Alcon Tears Carton
ALCON TEARS LUBRICANT EYE DROPS 
hypromellose 2910 solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0065-0408
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, Unspecified Form (UNII: GR686LBA74)  
Sodium Phosphate, Monobasic, Unspecified Form (UNII: 3980JIH2SW)  
Water (UNII: 059QF0KO0R)  
Sodium Chloride (UNII: 451W47IQ8X)  
Sodium Citrate, Unspecified Form (UNII: 1Q73Q2JULR)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0065-0408-721 in 1 CARTON03/01/2022
115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01803/01/2022
Labeler - Alcon Laboratories, Inc. (008018525)
Establishment
NameAddressID/FEIBusiness Operations
Alcon Research LLC007672236manufacture(0065-0408)

Revised: 12/2023
Document Id: ea6245c6-1d3b-4fac-a0b5-b576f9f53af5
Set id: 89302e2b-882b-48d5-8df7-be37859b48ba
Version: 3
Effective Time: 20231214
 
Alcon Laboratories, Inc.