Label: REFRESH TEARS- carboxymethylcellulose sodium solution/ drops
REFRESH TEARS- carboxymethylcellulose sodium kit

  • NDC Code(s): 0023-0795-65, 0023-0796-15, 0023-0797-05, 0023-0798-01, view more
    0023-0798-02, 0023-0798-03, 0023-0798-04, 0023-0798-15
  • Packager: Allergan, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated June 30, 2022

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  • 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. 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 tape seals on top and bottom flaps are intact.
    • Use before expiration date marked on container.
    • Discard 90 days after opening.
    • Store at 59°-77°F (15°-25°C).
    • RETAIN THIS CARTON FOR FUTURE REFERENCE.
  • Inactive ingredients

    Boric acid; calcium chloride dihydrate; magnesium chloride hexahydrate; potassium chloride; purified water; PURITE® (stabilized oxychloro complex); sodium borate decahydrate; and sodium chloride. May contain hydrochloric acid and/or sodium hydroxide (to adjust pH).

  • Questions or comments?

    1.800.678.1605

    refreshbrand.com

    v1.0DFL0798

  • PRINCIPAL DISPLAY PANEL

    Refresh
    Tears®
    Lubricant Eye Drops
    ORIGINAL STRENGTH
    Moisturizing Relief for
    Dry, Irritated Eyes
    0.5 fl oz (15 mL) Sterile

    Refresh Tears® Lubricant Eye Drops ORIGINAL STRENGTH Moisturizing Relief for Dry, Irritated Eyes 0.5 fl oz (15 mL) Sterile

  • PRINCIPAL DISPLAY PANEL

    Multi-Pack
    More bottles
    for more places
    Refresh
    Tears®
    Lubricant Eye Drops
    ORIGINAL STRENGTH
    Moisturizing Relief for
    Dry, Irritated Eyes
    4 bottles 0.5 fl oz (15 mL) each
    plus 1 bottle 0.17 fl oz (5 mL) Sterile

    Multi-Pack More bottles for more places Refresh Tears® Lubricant Eye Drops ORIGINAL STRENGTH Moisturizing Relief for Dry, Irritated Eyes 4 bottles 0.5 fl oz (15 mL) each plus 1 bottle 0.17 fl oz (5 mL) Sterile

  • INGREDIENTS AND APPEARANCE
    REFRESH TEARS 
    carboxymethylcellulose sodium solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0023-0798
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BORIC ACID (UNII: R57ZHV85D4)  
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORITE (UNII: G538EBV4VF)  
    SODIUM CHLORATE (UNII: T95DR77GMR)  
    CHLORINE DIOXIDE (UNII: 8061YMS4RM)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0023-0798-041 in 1 CARTON05/16/1997
    13 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    2NDC:0023-0798-031 in 1 CARTON05/16/1997
    23 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    3NDC:0023-0798-151 in 1 CARTON05/16/1997
    315 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    4NDC:0023-0798-012 in 1 CARTON05/16/1997
    415 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    5NDC:0023-0798-024 in 1 CARTON05/16/199701/27/2018
    515 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01805/16/1997
    REFRESH TEARS 
    carboxymethylcellulose sodium kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0023-0795
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0023-0795-651 in 1 CARTON01/01/2000
    11 in 1 TRAY; Type 1: Convenience Kit of Co-Package
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 14 BOTTLE, DROPPER 60 mL  in 4 
    Part 21 BOTTLE, DROPPER 5 mL
    Part 1 of 2
    REFRESH TEARS 
    carboxymethylcellulose sodium solution/ drops
    Product Information
    Item Code (Source)NDC:0023-0796
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BORIC ACID (UNII: R57ZHV85D4)  
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORITE (UNII: G538EBV4VF)  
    SODIUM CHLORATE (UNII: T95DR77GMR)  
    CHLORINE DIOXIDE (UNII: 8061YMS4RM)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0023-0796-1515 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01801/01/2000
    Part 2 of 2
    REFRESH TEARS 
    carboxymethylcellulose sodium solution/ drops
    Product Information
    Item Code (Source)NDC:0023-0797
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BORIC ACID (UNII: R57ZHV85D4)  
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORITE (UNII: G538EBV4VF)  
    SODIUM CHLORATE (UNII: T95DR77GMR)  
    CHLORINE DIOXIDE (UNII: 8061YMS4RM)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0023-0797-055 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01801/01/2000
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01801/01/2000
    Labeler - Allergan, Inc. (144796497)
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