Home > Drugs A-Z > REFRESH P.M.

REFRESH P.M. (Allergan, Inc.)

Available Formats

Dosage Form Package Information Links
OINTMENT 1 TUBE in 1 CARTON (0023-0240-04) > 3.5 g in 1 TUBE Label Information
OINTMENT 1 TUBE in 1 CARTON (0023-0240-21) > 3.5 g in 1 TUBE Label Information

Complete REFRESH P.M. Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • Active ingredients

    Mineral Oil 42.5%

    White Petrolatum 57.3%


  • Purpose

    Eye lubricant

    Eye 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

    • 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.


  • 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 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

  • Inactive ingredients

    Lanolin alcohols


  • Questions or comments?

    Telephone
1.800.433.8871

    refreshbrand.com


  • 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

    Carton

  • 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)