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retaine HPMC (OCuSOFT, Inc.)

Available Formats

Dosage Form Package Information Links
SOLUTION/ DROPS 10 mL in 1 BOTTLE, DROPPER (54799-896-10) Label Information

Complete retaine HPMC Information

  • Active Ingredient Hypromellose 0.3%


  • Purpose Eye lubricant


  • Uses  â–ª For the temporary releif of burning, irritation and discomfort due to dryness of the eye, or exposure to wind or sun. â–ª May be used as a protectant against further ittitation.

    Warnings
    â–ª For use in the eyes only. 


  • Do not use if solution changes color or becomes cloudy.

    When using this product
     â–ª do not touch tip of container to any surface to avoid contamination.
     â–ª replace cap after use.


  • Stop use and ask a doctor if â–ª you experience eye pain, changes in vision, continued redness or irritation of the eye. â–ª the 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 immediately.


  • Directions

    â–ª Instill 1 or 2 drops in the affected eye(s) as needed.


  • Other Information

    â–ª Use only it tamper seals on top ad bottom flaps are intact.
    â–ª Store between 15°-30°C (59°-86°F).
    â–ª Keep carton for complete product information.  
    â–ª Discard after 12 weeks.


  • Inactive ingredients

    Citric acid, sodium citrate, sorbitol, water for injection.


  • Questions?

    ☏(800)233-5469 M-F
    8:30AM-5:00PM CST
    www.retainebrand.com


  • Principal Display Panel

    HPMC


  • INGREDIENTS AND APPEARANCE
    RETAINE HPMC  
    hypromellose 2910 (4000 mpa.s) solution/ drops
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:54799-896
    Route of Administration OPHTHALMIC, TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Hypromellose 2910 (4000 Mpa.s) (UNII: RN3152OP35) (Hypromellose 2910 (4000 Mpa.s) - UNII:RN3152OP35) Hypromellose 2910 (4000 Mpa.s) 3 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    Anhydrous Citric Acid (UNII: XF417D3PSL)  
    Sodium Citrate (UNII: 1Q73Q2JULR)  
    Sorbitol (UNII: 506T60A25R)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:54799-896-10 10 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part349 05/01/2013
    Labeler - OCuSOFT, Inc. (174939207)
    Registrant - OCuSOFT, Inc. (174939207)