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Major LubriFresh PM by Preferred Pharmaceuticals Inc.

Medically reviewed on Jul 5, 2017

Dosage form: ointment
Ingredients: MINERAL OIL 150mg in 1g, PETROLATUM 830mg in 1g
Labeler: Preferred Pharmaceuticals Inc.
NDC Code: 68788-6987

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.

Active ingredients                                               Purpose

Mineral oil 15%...................................................Lubricant

White petrolatum 83%.........................................Lubricant

Uses

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

Warnings

When using this product

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
the condition worsens or persists more than 72 hours

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) and apply a small amount (1/4") of ointment to the inside of eyelid

Other information

store away from heat
protect from freezing
use before expiration date marked on container
store at 59°-86°F (15°-30°C)

Inactive ingredients

lanolin alcohol

Distributed by:

Major Pharmaceuticals

17177 N Laurel Park Dr.,

Suiet 233

Livonia, MI 48150

Made in Korea

Repackaged By: Preferred Pharmaceuticals Inc.

MAJOR LUBRIFRESH PM 
mineral oil and white petrolatum ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68788-6987(NDC:0904-6488)
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MINERAL OIL (MINERAL OIL) MINERAL OIL150 mg  in 1 g
PETROLATUM (PETROLATUM) PETROLATUM830 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
LANOLIN ALCOHOLS 
Packaging
#Item CodePackage Description
1NDC:68788-6987-31 TUBE in 1 CARTON
13.5 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34907/05/2017
Labeler - Preferred Pharmaceuticals Inc. (791119022)
Registrant - Preferred Pharmaceuticals Inc. (791119022)
Establishment
NameAddressID/FEIOperations
Preferred Pharmaceuticals Inc.791119022RELABEL(68788-6987)

 
Preferred Pharmaceuticals Inc.

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Further information

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

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