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REFRESH LIQUIGEL (Allergan, Inc.)

Available Formats

Dosage Form Package Information Links
SOLUTION/ DROPS 2 BOTTLE, DROPPER in 1 CARTON (0023-9205-02) > 15 mL in 1 BOTTLE, DROPPER Label Information
SOLUTION/ DROPS 1 BOTTLE, DROPPER in 1 CARTON (0023-9205-15) > 15 mL in 1 BOTTLE, DROPPER Label Information
SOLUTION/ DROPS 1 BOTTLE, DROPPER in 1 CARTON (0023-9205-03) > 3 mL in 1 BOTTLE, DROPPER Label Information

Complete REFRESH LIQUIGEL Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • Active ingredient

    Carboxymethylcellulose sodium 1%


  • 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. Replace cap after using.
    • 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

    Instill 1 or 2 drops in the affected eye(s) as needed.


  • Other information

    • Use only if imprinted tape seals on top and bottom flaps are intact and clearly legible.
    • Use before expiration date marked on container.
    • Discard 90 days after opening.
    • Store at 59°-86°F (15°-30°C).
    • RETAIN THIS CARTON FOR FUTURE REFERENCE.

  • Inactive ingredients

    Boric acid; calcium chloride; magnesium chloride; potassium chloride; purified water; PURITE® (stabilized oxychloro complex); sodium borate; and sodium chloride.


  • Questions or comments?

    Telephone
1.800.433.8871
    refreshbrand.com


  • PRINCIPAL DISPLAY PANEL

    Refresh
    Liquigel®
    Lubricant Eye Gel

    SOOTHING GEL

    Long-lasting relief
    for dry eyes in a
    soothing gel formula

    0.5 fl oz (15 mL) Sterile

    Carton

  • INGREDIENTS AND APPEARANCE
    REFRESH LIQUIGEL 
    carboxymethylcellulose sodium gel
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0023-9205
    Route of Administration OPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Carboxymethylcellulose sodium (UNII: K679OBS311) (Carboxymethylcellulose - UNII:05JZI7B19X) Carboxymethylcellulose sodium 10 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    Boric acid (UNII: R57ZHV85D4)  
    calcium chloride (UNII: M4I0D6VV5M)  
    magnesium chloride (UNII: 02F3473H9O)  
    potassium chloride (UNII: 660YQ98I10)  
    water (UNII: 059QF0KO0R)  
    sodium borate (UNII: 91MBZ8H3QO)  
    sodium chloride (UNII: 451W47IQ8X)  
    sodium chlorite (UNII: G538EBV4VF)  
    sodium chlorate (UNII: T95DR77GMR)  
    chlorine dioxide (UNII: 8061YMS4RM)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0023-9205-03 1 in 1 CARTON 10/04/2001
    1 3 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    2 NDC:0023-9205-15 1 in 1 CARTON 10/04/2001
    2 15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    3 NDC:0023-9205-02 2 in 1 CARTON 10/04/2001
    3 15 mL in 1 BOTTLE, DROPPER; 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 10/04/2001
    Labeler - Allergan, Inc. (144796497)
    Establishment
    Name Address ID/FEI Business Operations
    Allergan, Inc. 362898611 MANUFACTURE(0023-9205)