SYSTANE- hypromellose gel 
Alcon Laboratories, Inc.

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Drug Facts

Active ingredientPurpose
Hypromellose (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

carbopol 980, phosphonic acid, purified water, sodium perborate and sorbitol. May contain sodium hydroxide to adjust pH.

Questions?

In the U.S. call 1-800-757-9195
alcon.medinfo@alcon.com
www.systane.com

PRINCIPAL DISPLAY PANEL

Systane® 
LUBRICANT EYE GEL

NIGHT GEL

COMFORTING
DRY EYE RELIEF


Long lasting gel
for nighttime use


Soothing relief

#1 DOCTOR RECOMMENDED BRAND1
 
GEL

Alcon


STERILE 10g
(0.35 OZ)

TAMPER EVIDENT: For your
protection, use only if pull tab is
intact at time of purchase.

www.alconpatents.com

1 Based on a survey of eye care
professionals. Data on file.

Processed in France with
US-origin active ingredient for:
Alcon Laboratories, Inc.
Fort Worth, TX 76134 USA

25368501-0519

25368501

LOT / EXP

25368501-0519
SYSTANE 
hypromellose gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0065-0474
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 g
Inactive Ingredients
Ingredient NameStrength
Carbomer Homopolymer Type C (allyl Pentaerythritol Crosslinked) (UNII: 4Q93RCW27E)  
Phosphonic Acid (UNII: 35V6A8JW8E)  
Water (UNII: 059QF0KO0R)  
Sodium Perborate (UNII: Y52BK1W96C)  
Sorbitol (UNII: 506T60A25R)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0065-0474-011 in 1 CARTON12/15/2012
110 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:0065-0474-021 in 1 CARTON12/15/201212/31/2018
23.5 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01812/15/2012
Labeler - Alcon Laboratories, Inc. (008018525)
Establishment
NameAddressID/FEIBusiness Operations
Excelvision274234566manufacture(0065-0474) , label(0065-0474) , pack(0065-0474)
Establishment
NameAddressID/FEIBusiness Operations
SERVIPACK571772875label(0065-0474) , pack(0065-0474)

Revised: 12/2023
Document Id: 634b9bdb-004a-462e-ba48-1ab306157e02
Set id: 5f74b161-ae41-d0e2-6ed9-8deca55d2c0f
Version: 9
Effective Time: 20231215
 
Alcon Laboratories, Inc.