Label: SYSTANE- polyethylene glycol 400 and propylene glycol gel
- NDC Code(s): 0065-0454-07
- Packager: Alcon Laboratories, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 15, 2023
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- ACTIVE INGREDIENT
- Uses
- Warnings
- Do not use
- When using this product
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Questions?
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PRINCIPAL DISPLAY PANEL
Systane®
LUBRICANT EYE GEL
GEL DROPS
SOOTHING DRY EYE RELIEF
Long-lasting formula
Day or night protection
#1 DOCTOR RECOMMENDED BRAND1
LIQUID GEL
STERILE
10mL (1/3 FL OZ)
Alcon
SIDE PANEL
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.
www.alconpatents.com
Made in USA from domestic and imported materials
Indulge your eyes in this easy-to-use droppable gel. Systane® GEL DROPS forms a protective shield over your eyes to provide enduring relief day or night.
1 Based on a survey of eye care professionals. Data on file.
300048642-0621
Alcon
Alcon Laboratories, Inc.
Fort Worth, TX 76134 USA -
INGREDIENTS AND APPEARANCE
SYSTANE
polyethylene glycol 400 and propylene glycol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0065-0454 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Polyethylene Glycol 400 (UNII: B697894SGQ) (Polyethylene Glycol 400 - UNII:B697894SGQ) Polyethylene Glycol 400 4 mg in 1 mL Propylene Glycol (UNII: 6DC9Q167V3) (Propylene Glycol - UNII:6DC9Q167V3) Propylene Glycol 3 mg in 1 mL Inactive Ingredients Ingredient Name Strength Aminomethylpropanol (UNII: LU49E6626Q) Boric Acid (UNII: R57ZHV85D4) Edetate Disodium (UNII: 7FLD91C86K) Guaraprolose (3500 Mpa.S At 1%) (UNII: 3A1I7376TC) Polidronium Chloride (UNII: 6716Z5YR3G) Potassium Chloride (UNII: 660YQ98I10) Sodium Chloride (UNII: 451W47IQ8X) Sorbitol (UNII: 506T60A25R) Water (UNII: 059QF0KO0R) Hydrochloric Acid (UNII: QTT17582CB) Sodium Hydroxide (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0065-0454-07 10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 02/11/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M018 02/09/2011 Labeler - Alcon Laboratories, Inc. (008018525) Registrant - Alcon Laboratories, Inc. (008018525) Establishment Name Address ID/FEI Business Operations Alcon Research LLC 007672236 manufacture(0065-0454)