WALGREENS PM LUBRICANT EYE- mineral oil and white petrolatum ointment

Walgreens PM Lubricant Eye by

Drug Labeling and Warnings

Walgreens PM Lubricant Eye by is a Otc medication manufactured, distributed, or labeled by Walgreen Company, TRP Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

ACTIVE INGREDIENT

PURPOSE

• Active ingredients: Purpose
• Mineral Oil 3%: Lubricant
• White Petrolatum 94%: Lubricant

Uses

• for the temporary relief of dryness of the eye

Warnings

For use in eyes only
Retain outer carton for full product drug facts.

Do not use

Do not use if: you are sensitive to any ingredient in this product.

Stop use and ask a doctor

Stop use and ask a doctor if: You experience eye pain or change in vision, continued dryness or irritation of the eye. The condition worsens. Symptoms last longer than 72 hours.

KEEP OUT OF REACH OF CHILDREN

Keep this and all drugs out of the reach of children. If swallowed, get medical help or contact a Poison Control Center immediately (1-800-222-1222)

Directions

Directions

Pull down lower lid of the affected eye and apply a small amount (1/4 inch) of ointment to the inside of the eyelid, every 3-4 hours or as directed by doctor.

Other information

Do not use if bottom ridge of tube cap is exposed. Store at room temperature 15° to 30° C (59° to 86°F) Keep tube tightly closed.

See crimp of tube or box for lot number and expiration date.

Inactive ingredient

Lanolin alcohol.

Questions?

Questions or Comments?

1-800-925-4733 9am–5pm EST Monday–Friday

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WALGREENS PM LUBRICANT EYE 
mineral oil and white petrolatum ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-6855
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MINERAL OIL (UNII: T5L8T28FGP) (MINERAL OIL - UNII:T5L8T28FGP)	MINERAL OIL	30 mg  in 1 g
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	940 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: 0363-6855-13	1 in 1 CARTON	06/15/2021
1		3.5 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	06/15/2021

Labeler - Walgreen Company (008965063)

Registrant - TRP Company (105185719)