Available Formats

• SPL UNCLASSIFIED SECTION

  Drug Facts

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• Active ingredients

  Mineral Oil 42.5%

  White Petrolatum 57.3%

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• Purpose

  Eye lubricant

  Eye lubricant

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• 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.

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• 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 experience eye pain, changes in vision, continued redness or irritation of the eye, or if the 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 right away.

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• 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.

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• Other information

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

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• Inactive ingredients

  Lanolin alcohols

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• Questions or comments?

  1.800.433.8871

  refreshbrand.com

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• Principle Display Panel

  NDC 0023-0240-04

  Preservative-free

  Refresh

  P.M.®
  Lubricant Eye
  Ointment

  NIGHTTIME OINTMENT

  Protects the eyes
  from nighttime
  dryness and exposure

  Net wt. 0.12 oz (3.5 g) Sterile

  

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• INGREDIENTS AND APPEARANCE

  REFRESH P.M.  mineral oil, petrolatum ointment

  Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0023-0240 Route of Administration OPHTHALMIC

  Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength mineral oil (UNII: T5L8T28FGP) (mineral oil - UNII:T5L8T28FGP) mineral oil 425 mg  in 1 g petrolatum (UNII: 4T6H12BN9U) (petrolatum - UNII:4T6H12BN9U) petrolatum 573 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:0023-0240-21 1 in 1 CARTON 04/23/1990 1 3.5 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:0023-0240-04 1 in 1 CARTON 04/23/1990 2 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 04/23/1990

  Labeler - Allergan, Inc. (144796497)

  Establishment
  Name	Address	ID/FEI	Business Operations
  Allergan Sales, LLC		362898611	MANUFACTURE(0023-0240)

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