Label: BLINK TEARS- polyethylene glycol 400 solution/ drops

  • NDC Code(s): 29943-002-02, 29943-002-15, 29943-002-30
  • Packager: Bausch & Lomb Incorporated
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 20, 2025

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  • Active ingredient

    Polyethylene glycol 400 0.25%

  • Purpose

    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

    Do not use

    • if solution changes color or becomes cloudy

    When using this product

    • to avoid contamination, do not touch tip of container to any surface
    • remove contact lenses before using
    • replace cap after each use
  • Stop use and ask a doctor if

    • you experience eye pain, changes in vision, continued redness or irritation of the eye
    • 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 or as directed by your doctor
  • Other Information

    • store at 15-25 °C (59-77 °F)
  • Inactive ingredients

    boric acid; calcium chloride; magnesium chloride; potassium chloride; purified water; sodium borate; sodium chloride; sodium chloride as a preservative; sodium hyaluronate.

  • Questions or comments?

    [phone icon] call: 1-800-553-5340

  • Principal Display Panel - 15 mL Bottle Carton

    BAUSCH + LOMB

    blink ®
    tears

    Dry Eye
    Lubricating Eye Drops
    Mild-Moderate

    Long-Lasting Relief

    Instantly Soothes
    & Hydrates

    0.5 FL OZ (15 mL) STERILE

    carton
  • INGREDIENTS AND APPEARANCE
    BLINK TEARS 
    polyethylene glycol 400 solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29943-002
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 4002.5 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)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:29943-002-151 in 1 CARTON02/01/2008
    115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    2NDC:29943-002-301 in 1 CARTON02/01/2008
    230 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    3NDC:29943-002-021 in 1 CARTON02/01/2008
    32 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 DrugM01802/01/2008
    Labeler - Bausch & Lomb Incorporated (196603781)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bausch & Lomb Incorporated Greenville, South Carolina114406598manufacture(29943-002)
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