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Natural Balance Tears (Major Pharmaceuticals)

Available Formats

Dosage Form Package Information Links
SOLUTION/ DROPS 15 mL in 1 BOTTLE (0904-5018-35) Label Information

Complete Natural Balance Tears Information

  • Active ingredient

    Hypromellose 0.4%


  • Purpose

    Lubricant


  • Uses

    • to prevent further irritation

      to relieve dryness of the eye


  • Warnings

    Do not use if solution changes color or becomes cloudy

    When using this product  

    • do not touch tip of container to any surface to avoid contamination
    • 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
    • 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 to 2 drops in the affected eye(s) as needed

  • Other information

    • store at 15° - 30°C (59° - 86°F)
    • keep tightly closed

  • Inactive ingredients

    dibasic sodium phosphate, edetate disodium, monobasic sodium phosphate,

    potassium chloride, sodium chloride, purified water.

    Hydrochloric acid and/or sodium hydroxide may be added to adjust pH.

    PRESERVATIVE ADDED: benzalkonium chloride 0.01%


  • Questions ?

    Serious side effects associated with use of this product may be reported to 1800-323-0000

    ©Major Pharmaceuticals


  • Package/Label Principal Display Panel

    Carton

    NDC 0904-5018-35

    MAJOR®

    nature balance Tears

    Lubricant Eye Drops

    Sterile

    Relieves Dryness of the Eye

    Compare to Active Ingredient in Tears Naturale®*

    15 mL (1/2 FL. OZ.)


  • INGREDIENTS AND APPEARANCE
    NATURAL BALANCE TEARS 
    hypromellose solution/ drops
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0904-5018
    Route of Administration OPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HYPROMELLOSE 2910 (3 MPA.S) (UNII: 0VUT3PMY82) (HYPROMELLOSES - UNII:3NXW29V3WO) HYPROMELLOSE 2910 (3 MPA.S) 4 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    WATER (UNII: 059QF0KO0R)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0904-5018-35 15 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part349 10/07/2011
    Labeler - Major Pharmaceuticals (191427277)
    Establishment
    Name Address ID/FEI Business Operations
    Bausch & Lomb Incorporated 807927397 MANUFACTURE