Label: WALGREENS LUBRICANT EYE- carboxymethylcellulose sodium solution/ drops

  • 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 March 1, 2019

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Walgreens Lubricant Eye Drops

    Drug Facts

  • 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 use in the eyes only. 

    • Retain outer carton for full product drug facts.

  • Do not use

    • if solution changes color or becomes cloudy.

    When using this product

    • avoid contamination, do not touch tip of container to any surface. 

    • replace cap after use.

    Stop use and ask a doctor if

    • you experience eye pain, changes in vision, continued redness or irritation of the eye.

    • the condition worsens or persists for more than 72 hours.

    Keep this and all drugs out of the reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

  • Directions

    • Shake well before use.

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

  • Other information

    • store at room temperature 15°-30°C (59°-86°F)

    • keep tightly closed

  • Inactive ingredients

    Boric acid, calcium chloride, magnesium chloride, potassium chloride, sodium borate, sodium chloride, water for injection. Vanish® (Stabilized Peroxycomplex System as a preservative). May contain hydrochloric acid and/or sodium hydroxide to adjust pH.

  • Questions?

    1-800-925-4733 Monday thru Friday 8:30am - 5:00pm EST

  • PRINCIPAL DISPLAY PANEL

    Walgreens
    NDC 0363-0185-13
    Lubricant
    Eye Drops
    MOISTURIZING
    0.5 FL OZ (15 mL)

    Walgreens
NDC 0363-0185-13
Lubricant
Eye Drops
MOISTURIZING 
0.5 FL OZ (15 mL)

  • PRINCIPAL DISPLAY PANEL

    Walgreens
    NDC 0363-0185-49
    Lubricant
    Eye Drops
    MOISTURIZING
    2 BOTTLES 
    0.5 FL OZ (15 mL) EACH
    1.0 FL OZ (30ML) TOTAL

    Walgreens
NDC 0363-0185-49
Lubricant
Eye Drops
MOISTURIZING
2 BOTTLES 
0.5 FL OZ (15 mL) EACH
1.0 FL OZ (30ML) TOTAL

  • INGREDIENTS AND APPEARANCE
    WALGREENS LUBRICANT EYE 
    carboxymethylcellulose sodium solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0185
    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)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    WATER (UNII: 059QF0KO0R)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-0185-131 in 1 CARTON04/01/2019
    115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    2NDC:0363-0185-492 in 1 CARTON04/01/2019
    215 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 FINALpart34904/01/2019
    Labeler - Walgreen Company (008965063)