Label: REFRESH LIQUIGEL- carboxymethylcellulose sodium gel

  • NDC Code(s): 0023-9205-02, 0023-9205-03, 0023-9205-15
  • Packager: Allergan, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated November 11, 2022

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  • 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 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 or sodium hydroxide (to adjust pH).

  • Questions or comments?

    Telephone

    1.800.687.1605

    refreshbrand.com

    v1.0DFL9205

  • PRINCIPAL DISPLAY PANEL

    NDC 0023-9205-15

    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

    NDC 0023-9205-15 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

  • INGREDIENTS AND APPEARANCE
    REFRESH LIQUIGEL 
    carboxymethylcellulose sodium gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0023-9205
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Carboxymethylcellulose sodium (UNII: K679OBS311) (Carboxymethylcellulose - UNII:05JZI7B19X) Carboxymethylcellulose sodium10 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 borate (UNII: 91MBZ8H3QO)  
    sodium chloride (UNII: 451W47IQ8X)  
    sodium chlorite (UNII: G538EBV4VF)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0023-9205-031 in 1 CARTON10/04/200104/12/2020
    13 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    2NDC:0023-9205-151 in 1 CARTON10/04/2001
    215 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    3NDC:0023-9205-022 in 1 CARTON10/04/200104/12/2020
    315 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 finalpart34910/04/2001
    Labeler - Allergan, Inc. (144796497)
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