Label: CATACLENZ EYE RELIEF- calcarea carbonica, calcarea fluorica, causticum, cineraria maritima, euphrasia officinalis, naphthalinum, natrum muriaticum, phosphorus, quassia amara, silicea liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated October 29, 2015

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

  • ACTIVE INGREDIENT

    Drug Facts​__________________________________________________________________________________________________________

    HPUS active ingredients: Calcarea carbonica, Calcarea fluorica, Causticum, Cineraria maritima, Euphrasia officinalis, Naphthalinum, Natrum muriaticum, Phosphorus,  Quassia amara, Silicea​. Equal volumes of each ingredient in 10X, 30X, LM1 potencies.

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  • INDICATIONS & USAGE

    Uses ​for temporary relief from symptoms of common eye irritations: mineral accumulations, tearing, light sensitivity, eye fatigue, redness, itching.

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  • INACTIVE INGREDIENT

    Inactive Ingredients:

    Bio-Energetically Enhanced™ pure water, citric acid and potassium sorbate.

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  • WARNINGS

    Warnings

    • Stop use and ask your doctor if symptoms persist or worsen.
    • If pregnant or breast-feeding, ask a healthcare professional before use.
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  • KEEP OUT OF REACH OF CHILDREN

    • Keep out of reach of children.
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  • DOSAGE & ADMINISTRATION

    Directions

    • Initially, depress pump until primed.
    • Spray one dose directly into mouth.
    • Adults 12 and up: 3 sprays 3 times per day.
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  • OTHER SAFETY INFORMATION

    Tamper resistant for your protection. Use only if seal is intact.

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  • PURPOSE

    Uses for temporary relief from symptoms of common eye irritations:

    • mineral accumulations
    • tearing
    • light sensitivity
    • eye fatigue
    • redness
    • itching
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  • INGREDIENTS AND APPEARANCE
    CATACLENZ EYE RELIEF 
    calcarea carbonica, calcarea fluorica, causticum, cineraria maritima, euphrasia officinalis, naphthalinum, natrum muriaticum, phosphorus, quassia amara, silicea liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:57955-5112
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 10 [hp_X]  in 59 mL
    CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O) CALCIUM FLUORIDE 10 [hp_X]  in 59 mL
    CAUSTICUM (UNII: DD5FO1WKFU) (CAUSTICUM - UNII:DD5FO1WKFU) CAUSTICUM 10 [hp_X]  in 59 mL
    JACOBAEA MARITIMA (UNII: U4B223LS4X) (JACOBAEA MARITIMA - UNII:U4B223LS4X) JACOBAEA MARITIMA 10 [hp_X]  in 59 mL
    EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL) EUPHRASIA STRICTA 10 [hp_X]  in 59 mL
    NAPHTHALENE (UNII: 2166IN72UN) (NAPHTHALENE - UNII:2166IN72UN) NAPHTHALENE 10 [hp_X]  in 59 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 10 [hp_X]  in 59 mL
    PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 10 [hp_X]  in 59 mL
    QUASSIA AMARA WOOD (UNII: S5249Q85HW) (QUASSIA AMARA WOOD - UNII:S5249Q85HW) QUASSIA AMARA WOOD 10 [hp_X]  in 59 mL
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (COLLOIDAL SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 10 [hp_X]  in 59 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:57955-5112-2 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 10/28/2015
    Labeler - King Bio Inc. (617901350)
    Registrant - King Bio Inc. (617901350)
    Establishment
    Name Address ID/FEI Business Operations
    King Bio Inc. 617901350 manufacture(57955-5112)
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