Lubricant PM description, usages, side effects, indications, overdosage, supplying and lots more!

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Lubricant PM

Amerisource Bergen
Akorn, Inc.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active Ingredients

Mineral Oil 42.5% and

White Petrolatum 57.3%

Purpose

Lubricant

Uses

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

Warnings

  • For external use only.
  • To avoid contamination, do not touch tip of container to any surface. Replace cap after using.

Stop use and ask a doctor if

  • you feel eye pain
  • changes in vision occur
  • redness or irritation of the eye(s) gets worse, persists or lasts 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 and apply a small amount (one fourth inch) of ointment to the inside of the eyelid.

Other Information

  • Store away from heat.
  • Protect from freezing.
  • Use only if tape seals on top and bottom flaps are intact.
  • Use before expiration date marked on container.
  • Store at 15° to 30°C (59° to 86°F).
  • RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive Ingredient

Lanolin Alcohols

Questions or comments?

1-800-579-8327

*This product is not manufactured by Allergan, Inc., distributor of Refresh PM® Ointment

AMBRPC Rev. 01/13

Principal Display Panel Text for Container Label:

Good Neighbor Pharmacy Logo ® 46122-202-04

Lubricant PM Ointment

Mineral Oil, White Petrolatum Lubricant Eye Ointment

3.5 g (1/8 oz) Sterile

Principal Display Panel Text for Carton Label:

Compare to Refresh P.M.® Ointment active ingredients*

Good Neighbor Pharmacy Logo ® 46122-202-04

Lubricant PM Ointment

Mineral Oil, White Petrolatum Lubricant Eye Ointment

3.5 g (1/8 oz) Sterile

Lubricant PM

Mineral Oil, White Petrolatum OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:46122-202
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Mineral Oil 425 mg
petrolatum 573 mg

Inactive Ingredients

Ingredient Name Strength
Lanolin Alcohols

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 3.5 in 1 TUBE
2 NDC:46122-202-04 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2013-05-01


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Be sure to consult your doctor before taking any medication!
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