LUBRIFRESH PM- light mineral oil, white petrolatum ointment

LubriFresh PM by

Drug Labeling and Warnings

LubriFresh PM by is a Otc medication manufactured, distributed, or labeled by Major Pharmaceuticals, KC Pharmaceuticals, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Light Mineral Oil 15%

White Petrolatum 83%

PURPOSE

Eye Lubricant

INDICATIONS & USAGE

• for the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun
• may be used as a protectant against further irritation

DOSAGE & ADMINISTRATION

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

INACTIVE INGREDIENT

lanolin alcohols

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

WARNINGS

For external use only

When using this product

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

Stop use and ask a doctor if

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

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LUBRIFRESH PM 
light mineral oil, white petrolatum ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0904-7540
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIGHT MINERAL OIL (UNII: N6K5787QVP) (LIGHT MINERAL OIL - UNII:N6K5787QVP)	LIGHT MINERAL OIL	150 mg  in 1 g
WHITE PETROLATUM (UNII: B6E5W8RQJ4) (WHITE PETROLATUM - UNII:B6E5W8RQJ4)	WHITE PETROLATUM	830 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
LANOLIN ALCOHOLS (UNII: 884C3FA9HE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0904-7540-12	1 in 1 BOX	07/21/2025
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 Drug	M018	07/21/2025

Labeler - Major Pharmaceuticals (191427277)

Registrant - KC Pharmaceuticals, Inc (174450460)