Lubricant Eye

Dosage form: ointment
Ingredients: Mineral Oil 120mg in 1g, Petrolatum 880mg in 1g
Labeler: Akorn, Inc.
NDC code: 17478-063

Medically reviewed by Drugs.com. Last updated on Sep 25, 2023.

Drug Facts

Active ingredient

Mineral Oil

12%

White Petrolatum

88%

Contains no preservatives or lanolin.

Purpose

Eye lubricant

Uses

For use as a lubricant for the temporary relief of burning and irritation due to dryness of the eyes.

Warnings

Do not use if bottom ridge of tube is exposed.
To avoid contamination, do not touch tip of container to any surface.
Replace cap after using.

Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours.

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Pull down lower lid of the affected eye(s) and apply small amount (one-fourth inch) of ointment to the inside of the eyelid, one or more times daily, or as directed by a doctor.

Other information

Store at 20° to 25°C (68° to 77°F)
[see USP Controlled Room Temperature].
Store away from heat.
Protect from freezing.
Keep tightly closed.
See crimp for Control Number and Expiration Date.
RETAIN THIS CARTON FOR FUTURE REFERENCE.

NJTROAC Rev. 06/12

Principal Display Panel Text for Container Label:

NDC 17478-063-35 Akorn Logo

Lubricant Eye OINTMENT

Nighttime Relief For Dry Eyes Sterile

FOR OPHTHALMIC USE ONLY Net Wt. 3.5 g (1/8oz.)

Principal Display Panel Text for Carton Label:

NDC 17478-063-35

3.5 g

Lubricant

Eye

OINTMENT

Nighttime Relief

For Dry Eyes

Nighttime Relief

Plus Protection

Sterile

Net Wt. 3.5 g (1/8oz.)

LUBRICANT EYE
mineral oil and petrolatum ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:17478-063
Route of Administration	OPHTHALMIC	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Mineral Oil (Mineral Oil)	Mineral Oil	120 mg in 1 g
Petrolatum (Petrolatum)	Petrolatum	880 mg in 1 g

Packaging
#	Item Code	Package Description
1	NDC:17478-063-35	1 TUBE in 1 CARTON
1		3.5 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	04/01/1993

Labeler - Akorn, Inc. (062649876)

Establishment
Name	Address	ID/FEI	Operations
Akorn, Inc		603980319	MANUFACTURE(17478-063), ANALYSIS(17478-063), STERILIZE(17478-063), PACK(17478-063), LABEL(17478-063)

Revised: 10/2012

Document Id: a63c9756-ebd7-437c-8082-f24564a63a3e

Set id: b086dc94-ff35-43c6-a5a0-8a25d6104d61

Version: 2

Effective Time: 20121004

Akorn, Inc.

Further information

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

Medical Disclaimer