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Refresh Optive Sensitive (Allergan, Inc.)

Available Formats

Dosage Form Package Information Links
SOLUTION/ DROPS 60 VIAL, SINGLE-USE in 1 CARTON (0023-3416-60) > .4 mL in 1 VIAL, SINGLE-USE Label Information
SOLUTION/ DROPS 5 VIAL, SINGLE-USE in 1 CARTON (0023-3416-05) > .4 mL in 1 VIAL, SINGLE-USE Label Information
SOLUTION/ DROPS 30 VIAL, SINGLE-USE in 1 CARTON (0023-3416-30) > .4 mL in 1 VIAL, SINGLE-USE Label Information

Complete Refresh Optive Sensitive Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • Active ingredients

    Carboxymethylcellulose sodium 0.5%

    Glycerin 0.9%


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

    *lf 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

    Boric acid; calcium chloride dihydrate; erythritol; levocarnitine; magnesium chloride hexahydrate; potassium chloride; purified water; sodium borate decahydrate; and sodium citrate dihydrate.


  • Questions or comments?

    ☎ 1.800.678.1605

    refreshbrand.com


  • PRINCIPAL DISPLAY PANEL

    NDC 0023-3416-30

    Preservative-free

    Refresh
    Optive
    ®
    Lubricant Eye Drops

    LONG-LASTING HYDRATION

    Lubricating and hydrating formula
    penetrates the surface to relieve dryness.
    Also recommended for LASIK dryness.*

    30 Single-Use Containers
    0.01 fl oz (0.4 mL) each Sterile

    Carton

  • INGREDIENTS AND APPEARANCE
    REFRESH OPTIVE 
    carboxymethylcellulose sodium, glycerin solution/ drops
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0023-3416
    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
    Glycerin (UNII: PDC6A3C0OX) (Glycerin - UNII:PDC6A3C0OX) Glycerin 9 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    Boric Acid (UNII: R57ZHV85D4)  
    Calcium Chloride (UNII: M4I0D6VV5M)  
    Erythritol (UNII: RA96B954X6)  
    Levocarnitine (UNII: 0G389FZZ9M)  
    Magnesium Chloride (UNII: 02F3473H9O)  
    potassium chloride (UNII: 660YQ98I10)  
    water (UNII: 059QF0KO0R)  
    sodium borate (UNII: 91MBZ8H3QO)  
    trisodium citrate dihydrate (UNII: B22547B95K)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0023-3416-05 5 in 1 CARTON 08/22/2008
    1 0.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
    2 NDC:0023-3416-30 30 in 1 CARTON 08/22/2008
    2 0.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
    3 NDC:0023-3416-60 60 in 1 CARTON 08/22/2008
    3 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 08/22/2008
    Labeler - Allergan, Inc. (144796497)
    Establishment
    Name Address ID/FEI Business Operations
    Allergan Pharmaceuticals Ireland 219682291 MANUFACTURE(0023-3416)