Label: ADVANCED EYE RELIEF DRY EYE REJUVENATION- glycerin propylene glycol solution/ drops

  • NDC Code(s): 24208-454-30, 24208-454-32
  • Packager: Bausch & Lomb Incorporated
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 25, 2024

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  • Active ingredients

    Glycerin (0.3%)

    Propylene glycol (1.0%)

  • Purpose

    Lubricant

    Lubricant

  • Uses

    • temporary relief of burning and irritation due to dryness of the eye
    • prevents further irritation
  • Warnings

    For external use only

    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
    • remove contact lenses before using
    • 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 or 2 drops in the affected eye(s) as needed
  • Other information

    • store at 15–25°C (59–77 °F)
    • keep tightly closed
    • use before expiration date marked on the carton and bottle
  • Inactive ingredients

    benzalkonium chloride, boric acid, edetate disodium, potassium chloride, purified water, sodium borate, sodium chloride. Hydrochloric acid and/or sodium hydroxide may be used to adjust pH.

  • Questions or comments?

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

    Marketed by:
    Bausch & Lomb Americas Inc.
    Bridgewater, NJ 08807 USA

  • Package/Label Principal Display Panel

    carton

    BAUSCH + LOMB

    ADVANCED
    Eye Relief ®

    Dry Eye
    LUBRICANT EYE DROPS

    • Fast relief from dry eyes
    • Replenishes tears
    • Rejuvenates eyes

    STERILE 1.0 FL OZ (30 mL)

    6319221

  • INGREDIENTS AND APPEARANCE
    ADVANCED EYE RELIEF DRY EYE REJUVENATION 
    glycerin propylene glycol solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24208-454
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN3 mg  in 1 mL
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    BORIC ACID (UNII: R57ZHV85D4)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:24208-454-321 in 1 CARTON09/01/2010
    115 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:24208-454-301 in 1 CARTON05/01/2017
    230 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01809/01/2010
    Labeler - Bausch & Lomb Incorporated (196603781)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bausch & Lomb Incorporated114406598manufacture(24208-454)
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