Label: ROHTO HYDRA- hydroxyethyl cellulose (2000 mpa.s at 1%) liquid 

  • Label RSS
  • NDC Code(s): 10742-8148-1
  • Packager: The Mentholatum Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 01/14

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

  • Active ingredient

    Hydroxyethyl cellulose 0.6%

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  • Purpose

    Hydroxyethyl cellulose - Lubricant

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  • Uses

    temporarily relieves discomfort due to minor irritations of the eye or exposure to wind or sun
    lubricates to prevent further irritation or to relieve dryness of the eye
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  • Warnings

    For external use only

    When using this product

    do not touch tip of container to any surface to avoid contamination
    replace cap after each use
    do not use if solution changes color or becomes cloudy
    remove contact lenses before using

    Stop use and ask a doctor if

    you feel eye pain
    changes in vision occur
    redness or irritation of the eyes lasts
    condition worsens or lasts more than 72 hours

    Keep out of reach of children.

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

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  • Directions

    put 1 or 2 drops in the affected eye(s) as needed

    Other information

    store at 20-25 °C (68-77°F)
    tightly snap on cap to seal
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  • Inactive ingredients

    boric acid, edetate disodium, menthol, polysorbate 80, potassium chloride, purified water, sodium borate, sodium chloride, sodium chondroitin sulfate

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  • Questions?

    Toll free 1-877-636-2677 MON-FRI 9AM to 5PM (EST) consumeraffairs@mentholatum.com

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  • INGREDIENTS AND APPEARANCE
    ROHTO HYDRA 
    hydroxyethyl cellulose liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:10742-8148
    Route of Administration OPHTHALMIC DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)) HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) 6 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    BORIC ACID  
    EDETATE DISODIUM  
    MENTHOL  
    POLYSORBATE 80  
    POTASSIUM CHLORIDE  
    WATER  
    SODIUM BORATE  
    SODIUM CHLORIDE  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:10742-8148-1 1 in 1 CARTON
    1 13 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part349 01/03/2011
    Labeler - The Mentholatum Company (002105757)
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