Label: AUROVISC LUBRICANT HYPROMELLOSE 2208 (15000 MPA.S) GEL/DROPS- hypromellose ophthalmic solution 2% w/v solution, gel forming / drops

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 12, 2024

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  • ACTIVE INGREDIENT

    Hypromellose USP 2% w/v

  • INACTIVE INGREDIENT

    1. Acetic acid 1%
    2. Calcium chloride
    3. Citric acid 0.1465%
    4. Magnesium Chloride
    5. Sodium chloride
    6. Sodium acetate,
    7. Sodium Citrate
    8. Potassium chloride
    9. Purified water.
  • USE

    For use as a lubricant to prevent further irritation or to relieve dryness of the eye

  • QUESTIONS

    Call. 1-800-103-7321,

    E-mail : info@aurolab.com
    Web : www.aurolab.com

  • KEEP OUT OF REACH OF CHILDREN

    If swallowed get medical help or contact a Poison Control Center right away.

  • STOP USE

    1. Transient blurring of vision
    2. Ocular discomfort or irritation
    3. Matting or Stickness of eyelashes
    4. Photophobia
    5. Hypersensitivity or edema of the eyelids
  • DO NOT USE

    1. If the solution becomes dark brown or any floating particles are observed.
    2. If you are sensitive to any ingredient in this product
  • WARNINGS

    For External use only

  • INDIACATIONS AND USAGE

    Do not use if package is damaged
    Discard after a single use
    Do not freeze
    Do not resterilize

  • Purpose

    Lubricant

  • Dose

    Instill 1 or 2 drops in the affected eyes as needed

  • PACKAGE CARTON

    HPMC

  • INGREDIENTS AND APPEARANCE
    AUROVISC LUBRICANT HYPROMELLOSE 2208 (15000 MPA.S) GEL/DROPS 
    hypromellose ophthalmic solution 2% w/v solution, gel forming / drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:16030-303
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPROMELLOSE 2208 (15000 MPA.S) (UNII: Z78RG6M2N2) (HYPROMELLOSE 2208 (15000 MPA.S) - UNII:Z78RG6M2N2) HYPROMELLOSE 2208 (15000 MPA.S)20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SODIUM ACETATE (UNII: 4550K0SC9B)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    CITRIC ACID ACETATE (UNII: DSO12WL7AU)  
    ACETIC ACID (UNII: Q40Q9N063P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:16030-303-022 mL in 1 SYRINGE, GLASS; Type 1: Convenience Kit of Co-Package09/26/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01809/26/2022
    Labeler - Aurolab (677319965)
    Establishment
    NameAddressID/FEIBusiness Operations
    Aurolab677319965manufacture(16030-303)
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