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REFRESH PLUS (Allergan, Inc.)

Available Formats

Dosage Form Package Information Links
SOLUTION/ DROPS 5 VIAL, SINGLE-USE in 1 CARTON (0023-0403-05) > .4 mL in 1 VIAL, SINGLE-USE Label Information
SOLUTION/ DROPS 50 VIAL, SINGLE-USE in 1 CARTON (0023-0403-50) > .4 mL in 1 VIAL, SINGLE-USE Label Information
SOLUTION/ DROPS 100 VIAL, SINGLE-USE in 1 CARTON (0023-0403-10) > .4 mL in 1 VIAL, SINGLE-USE Label Information
SOLUTION/ DROPS 30 VIAL, SINGLE-USE in 1 CARTON (0023-0403-30) > .4 mL in 1 VIAL, SINGLE-USE Label Information
SOLUTION/ DROPS 70 VIAL, SINGLE-USE in 1 CARTON (0023-0403-70) > .4 mL in 1 VIAL, SINGLE-USE Label Information

Complete REFRESH PLUS Information

  • Active ingredient

    Carboxymethylcellulose sodium 0.5%


  • Purpose

    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. Do not reuse. Once opened, discard.
    • Do not touch unit-dose tip to eye.
    • If solution changes color or becomes cloudy, do not use.

    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

    To open, TWIST AND PULL TAB TO REMOVE. Instill 1 or 2 drops in the affected eye(s) as needed and discard container.

    *If used for post-operative (e.g., LASIK) dryness and discomfort, follow your eye doctor’s instructions.


  • Other information   

    • Use only if single-use container is intact.
    • Use before expiration date marked on container.
    • Store at 59°-86°F (15°-30°C).
    • RETAIN THIS CARTON FOR FUTURE REFERENCE.

  • Inactive ingredients

    Calcium chloride; magnesium chloride; potassium chloride; purified water; sodium chloride; and sodium lactate. May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.


  • Questions or comments?

    1.800.433.8871

    refreshbrand.com


  • PRINCIPAL DISPLAY PANEL

    NDC 0023-0403-30
    Preservative-free
    Refresh
    Plus
    Lubricant Eye Drops
    MOISTURIZING RELIEF 
    Immediate, soothing relief
    for dry eyes. Also recommended
    for LASIK dryness*
    30 Single-Use Containers
    0.01 fl oz (0.4 mL) each Sterile

    PRINCIPAL DISPLAY PANEL
NDC 0023-0403-30
Preservative-free
Refresh
Plus
Lubricant Eye Drops
MOISTURIZING RELIEF 
Immediate, soothing relief 
for dry eyes. Also recommended 
for LASIK dryness*
30 Single-Use Containers
0.01 fl oz (0.4 mL) each Sterile


  • PRINCIPAL DISPLAY PANEL

    NDC 0023-0403-30
    Preservative-free
    Refresh
    Plus
    Lubricant Eye Drops
    MOISTURIZING RELIEF
    Immediate, soothing relief
    for dry eyes. Also recommended
    for LASIK dryness*
    30 Single-Use Containers
    0.01 fl oz (0.4 mL) each Sterile

    PRINCIPAL DISPLAY PANEL
NDC 0023-0403-30
Preservative-free
Refresh
Plus
Lubricant Eye Drops
MOISTURIZING RELIEF 
Immediate, soothing relief 
for dry eyes. Also recommended 
for LASIK dryness*
30 Single-Use Containers
0.01 fl oz (0.4 mL) each Sterile


  • INGREDIENTS AND APPEARANCE
    REFRESH PLUS 
    carboxymethylcellulose sodium solution/ drops
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0023-0403
    Route of Administration OPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM 5 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM LACTATE (UNII: TU7HW0W0QT)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0023-0403-05 5 in 1 CARTON 10/09/1996
    1 0.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
    2 NDC:0023-0403-30 30 in 1 CARTON 10/09/1996
    2 0.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
    3 NDC:0023-0403-50 50 in 1 CARTON 10/09/1996
    3 0.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
    4 NDC:0023-0403-70 70 in 1 CARTON 10/09/1996
    4 0.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
    5 NDC:0023-0403-10 100 in 1 CARTON 10/09/1996
    5 0.4 mL in 1 VIAL, SINGLE-USE; 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 10/09/1996
    Labeler - Allergan, Inc. (144796497)