HYLATEARS (EYE DROPS) LIQUID [HYALOGIC LLC]

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HYLATEARS (EYE DROPS) LIQUID [HYALOGIC LLC]
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NDC 72094-001-01
Set ID 64a30066-79a2-451d-e053-2991aa0ac68c
Category HUMAN OTC DRUG LABEL
Packager Hyalogic LLC
Generic Name
Product Class
Product Number
Application Number PART349
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  • ACTIVE INGREDIENT

    active ingredient

  • KEEP OUT OF REACH OF CHILDREN

    Keep Out of reach of children

  • DOSAGE & ADMINISTRATION

    Directions

  • WARNINGS

    warnings

  • INACTIVE INGREDIENT

    Inactive Ingredients

  • INDICATIONS & USAGE

    Uses

  • PURPOSE

    Purpose

  • HylaTears Updated Box

    Final Box

  • INGREDIENTS AND APPEARANCE
    HYLATEARS 
    eye drops liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72094-001
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPROMELLOSE 2910 (4000 MPA.S) (UNII: RN3152OP35) (HYPROMELLOSE 2910 (4000 MPA.S) - UNII:RN3152OP35) HYPROMELLOSE 2910 (4000 MPA.S)3 mg  in 10 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    SODIUM PHOSPHATE DIBASIC DIHYDRATE (UNII: 94255I6E2T)  
    SODIUM PHOSPHATE LINKAGE (UNII: M895BOC3WI)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72094-001-0120 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product02/12/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34902/12/2018
    Labeler - Hyalogic LLC (026884299)
    Registrant - Regulatory Matters Consulting (080711165)
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