DRY EYES- white petrolatum mineral oil ointment

Dry Eyes by

Drug Labeling and Warnings

Dry Eyes by is a Otc medication manufactured, distributed, or labeled by Cardinal Health, Bausch & Lomb Incorporated. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Mineral oil 15%
White petrolatum 83%

Purpose

Lubricant

Uses

• to prevent further irritation
• to relieve dryness of the eye

Warnings

When using this product  

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

Stop use and ask a doctor if

• condition worsens or persists for more than 72 hours
• you experience eye pain, changes in vision, continued redness or irritation of the eye

Keep out of reach of children.

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

Directions

•   pull down the lower lid of the affected eye(s)
•   apply a small amount (1/4 inch) of ointment to the inside of eyelid
•   apply one or more times daily or as directed by a doctor

Other information

• store at 15° - 30°C (59° - 86°F)
• keep tightly closed
• see crimp of tube or carton for Lot Number and Expiration Date

 

Inactive ingredient

lanolin oil

Questions?

Serious side effects associated with use of this product may be reported to

1-800-323-0000

DO NOT USE IF CAP AND NECKRING ARE NOT INTACT.

Package/Label Principal Display Panel

NDC: 37205-134-79

LEADER®

Compare to Refresh P.M. active ingredient*

Dry Eyes

Lubricant Eye Ointment
(Sterile)

Preservative Free

Prevents irritation & relieves dryness of the eye

SATISFACTION GUARANTEED Net wt. 1/8 oz. (3.5 g)

INGREDIENTS AND APPEARANCE

DRY EYES 
white petrolatum mineral oil ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37205-134
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MINERAL OIL (UNII: T5L8T28FGP) (MINERAL OIL - UNII:T5L8T28FGP)	MINERAL OIL	150 mg  in 1 g
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	830 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
LANOLIN (UNII: 7EV65EAW6H)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37205-134-79	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	11/15/2011

Labeler - Cardinal Health (097537435)

Registrant - Bausch & Lomb Incorporated (196603781)

Establishment
Name	Address	ID/FEI	Business Operations
Bausch & Lomb Incorporated		807927397	MANUFACTURE