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LubriFresh P.M. by Preferred Pharmaceuticals Inc.

Dosage form: ointment
Ingredients: MINERAL OIL 150mg in 1g, PETROLATUM 830mg in 1g
Labeler: Preferred Pharmaceuticals Inc.
NDC Code: 68788-9973

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Artificial Tears Ointment Drug Facts

Active ingredient

Mineral oil 15%
White petrolatum 83%



to prevent further irritation
to relieve dryness of the eye


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.

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 or comments?

Serious side effects associated with use of this product may be reported to 1800-323-0000

*Major LubriFreshTM P.M. is not manufactured or distributed by Allergan Inc., distributor of Refresh P.M.®

Relabeled by: Preferred Pharmaceuticals Inc.

Package/Label Principal Display Panel

NDC -68788-9973-3

LubriFreshTM P.M.

Lubricant Eye Ointment (Sterile)


Prevents Irritation and Relieves Dryness of the eye

Compare to Active Ingredients of Refresh P.M.®*

Net Wt. 1/8 oz (3.5 g)

white petrolatum mineral oil ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68788-9973(NDC:0904-5168)
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:68788-9973-33.5 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34905/07/2015
Labeler - Preferred Pharmaceuticals Inc. (791119022)
Registrant - Preferred Pharmaceuticals Inc. (791119022)
Preferred Pharmaceuticals Inc.791119022RELABEL(68788-9973)

Revised: 12/2017
Preferred Pharmaceuticals Inc.

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.