Label: REFRESH OPTIVE- carboxymethylcellulose sodium, glycerin solution/ drops

  • NDC Code(s): 0023-3416-05, 0023-3416-30, 0023-3416-60
  • Packager: Allergan, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 23, 2022

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  • 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. *Follow your eye doctor’s instructions if you are using this product after an eye surgery (e.g., LASIK) to relieve eye dryness and discomfort.

  • Other information

    • Use only if single-use container is intact.
    • Use before expiration date marked on container.
    • Store at 59°-77°F (15°-25°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

    v1.0DFL3416

  • 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 Vials 0.01 fl oz (0.4 mL) each Sterile

    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 Vials 0.01 fl oz (0.4 mL) each Sterile

  • INGREDIENTS AND APPEARANCE
    REFRESH OPTIVE 
    carboxymethylcellulose sodium, glycerin solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0023-3416
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Carboxymethylcellulose Sodium (UNII: K679OBS311) (Carboxymethylcellulose - UNII:05JZI7B19X) Carboxymethylcellulose Sodium5 mg  in 1 mL
    Glycerin (UNII: PDC6A3C0OX) (Glycerin - UNII:PDC6A3C0OX) Glycerin9 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0023-3416-055 in 1 CARTON08/22/2008
    10.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
    2NDC:0023-3416-3030 in 1 CARTON08/22/2008
    20.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
    3NDC:0023-3416-6060 in 1 CARTON08/22/2008
    30.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01808/22/2008
    Labeler - Allergan, Inc. (144796497)
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