Lubricant Eye Drops

Dosage form: solution/ drops
Ingredients: Polyethylene Glycol 400 4mg in 1mL, Propylene Glycol 3mg in 1mL
Labeler: Chain Drug Consortium
NDC code: 68016-404

Medically reviewed by Drugs.com. Last updated on Oct 14, 2024.

Drug Facts

Active ingredients

Polyethylene Glycol 400 0.4%

Propylene Glycol 0.3%

Purpose

Lubricant

Uses

For the temporary relief of burning and irritation due to dryness of the eye.

Warnings

For external use only.

Do not use

if this product changes color or becomes cloudy
if you are sensitive to any ingredient in this product

When using this product

do not touch tip of container to any surface to avoid contamination
replace cap after each use

Stop use and ask a doctor if

you feel eye pain
changes in vision occur
redness or irritation of the eye(s) gets worse, persists or lasts more than 72 hours

Keep out of reach of children.

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

Directions

instill 1 or 2 drops in the affected eye(s) as needed

Other information

store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].

Inactive ingredients

Purified Water, Boric Acid, Hypromellose, Sodium Chloride, Potassium Chloride, Zinc Chloride, Calcium Chloride Dihydrate, Magnesium Chloride Hexahydrate. May contain Hydrochloric Acid and/or Sodium Hydroxide to adjust pH;

Preservative

Benzalkonium Chloride.

Questions or comments?

1-800-932-5676

Principal Display Panel Text for Container Label:

68016-404-00

Premier

Value® Logo

Lubricant

Eye Drops

PEG-PHEN

LUBRICANT

EYE DROPS

Long lasting
Soothing comfort dry eye therapy

15 mL (0.5 FL OZ) STERILE

Principal Display Panel Text for Carton Label:

68016-404-00

*COMPARE TO THE

ACTIVE INGREDIENT

IN SYSTANE®

Premier

Value ® Logo

Lubricant

Eye Drops

PEG-PHEN

LUBRICANT

EYE DROPS

Long lasting
Soothing comfort

dry eye therapy

15 mL (0.5 FL OZ)

STERILE PV Brand Logo

LUBRICANT EYE DROPS
polyethylene glycol 400 and propylene glycol solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:68016-404
Route of Administration	OPHTHALMIC	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Polyethylene Glycol 400 (Polyethylene Glycol 400)	Polyethylene Glycol 400	4 mg in 1 mL
Propylene Glycol (Propylene Glycol)	Propylene Glycol	3 mg in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water
Boric Acid
Hypromelloses
Sodium Chloride
Potassium Chloride
Zinc Chloride
Calcium Chloride
Magnesium Chloride
Hydrochloric Acid
Sodium Hydroxide
Benzalkonium Chloride

Packaging
#	Item Code	Package Description
1	NDC:68016-404-00	1 BOTTLE, DROPPER in 1 CARTON
1		15 mL in 1 BOTTLE, DROPPER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	01/10/2014

Labeler - Chain Drug Consortium (101668460)

Registrant - Akorn, Inc. (062649876)

Establishment
Name	Address	ID/FEI	Operations
Akorn, Inc		603980319	MANUFACTURE(68016-404), ANALYSIS(68016-404), STERILIZE(68016-404), PACK(68016-404), LABEL(68016-404)

Revised: 10/2015

Document Id: 4afaac05-13de-42d2-b6ee-f817443721d9

Set id: ffe98484-20b7-4578-b9cc-0707f8e3d2b1

Version: 2

Effective Time: 20151023

Chain Drug Consortium

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer