Label: EQUATE EYE DROPS DRY EYE RELIEF- glycerin, hypromellose, polyethylene glycol 400 solution/ drops

  • NDC Code(s): 49035-280-01, 49035-280-02
  • Packager: Wal-Mart Stores, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 23, 2023

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

  • Active ingredients

    Glycerin 0.2%

    Hypromellose 0.2%

    Polyethylene glycol 400 1%

  • Purposes

    Lubricant

    Lubricant

    Lubricant

  • Uses

    • for protection against further irritation
    • for temporary relief of burning and irritation due to dryness of the eye
  • Warnings

    For external use only

    Do not use this product if

    solution changes color or becomes cloudy

    When using this product

    • to avoid contamination, do not touch tip of container to any surface. Replace cap after using.
    • remove contact lenses before using

    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

    If pregnant or breast-feeding,

    ask a health professional before use.

    Keep out of reach of children.

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

  • Inactive ingredients

    benzalkonium chloride, dextrose, edetate disodium, potassium chloride, purified water, sodium bicarbonate, sodium chloride, sodium citrate, sodium phosphate dibasic, sodium phosphate monobasic

  • Questions or comments?

    1-888-287-1915

  • Equate Dry Eye Relief Eye Drops 2-0.5oz bottles

    Equate Dry Eye Relief Eye Drops 2-0.5oz bottles

  • Equate Eye Drops Dry Eye Relief 2-0.5oz bottles

    Equate Eye Drops Dry Eye Relief 2-0.5oz bottles

  • INGREDIENTS AND APPEARANCE
    EQUATE EYE DROPS DRY EYE RELIEF 
    glycerin, hypromellose, polyethylene glycol 400 solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-280
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN0.2 g  in 100 mL
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) (HYPROMELLOSE, UNSPECIFIED - UNII:3NXW29V3WO) HYPROMELLOSE, UNSPECIFIED0.2 g  in 100 mL
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL, UNSPECIFIED - UNII:3WJQ0SDW1A) POLYETHYLENE GLYCOL 4001 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS (UNII: KH7I04HPUU)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    SODIUM PHOSPHATE DIBASIC DIHYDRATE (UNII: 94255I6E2T)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    DEXTROSE (UNII: IY9XDZ35W2)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49035-280-012 in 1 BOX11/01/2019
    115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    2NDC:49035-280-022 in 1 BOX02/01/2021
    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 DrugM01811/01/2019
    Labeler - Wal-Mart Stores, Inc. (051957769)
    Registrant - KC Pharmaceuticals, Inc. (174450460)
    Establishment
    NameAddressID/FEIBusiness Operations
    KC Pharmaceutical, Inc.174450460manufacture(49035-280) , pack(49035-280) , label(49035-280)