Label: EUPHRASIA OFFICINALIS- euphrasia tablet

  • NDC Code(s): 0360-0172-01
  • Packager: STANDARD HOMEOPATHIC COMPANY
  • 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 December 13, 2018

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

  • SPL UNCLASSIFIED SECTION

    Made according to the
    Homeopathic Pharmacopoeia
    of the United States since 1903.

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  • Warnings

    Do not use if cap band is missing or broken.

    If you are pregnant or nursing, consult a licensed health
    care professional before using this product.

    If symptoms persist for 7 days or worsen,
    contact a licensed practitioner.

    Keep this and all medicines out of the reach of children.

    To be used according to label indications and/or
    standard homeopathic indications.

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  • QUESTIONS

    Standard Homeopathic Company
    Los Angeles, CA 90061
    Questions? 800-624-9659

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  • Directions

    Adults: Dissolve 4 tablets under tongue 4 times a day.
    Children: Consult a healthcare professional

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  • INACTIVE INGREDIENT

    In a base of Acacia Gum and Lactose N.F.

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  • ACTIVE INGREDIENT

    EUPHRASIA 6X

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  • INDICATIONS & USAGE

    EYE IRRITATION, COLD OR HAY FEVER

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  • Principal Display Panel -- 250 Tablet Bottle Label

    Standard

    Homeopathic
    Made in the USA Since 1903

    NDC # 0360-0172-01

    Homeopathic Medicine

    EUPHRASIA

    6X

    EYE IRRITATION, COLD OR

    HAY FEVER*

    *Claims based on traditional homeopathic

    practice, not accepted medical evidence.

    Not FDA evaluated.


    250 TABLETS

    Label

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  • INGREDIENTS AND APPEARANCE
    EUPHRASIA OFFICINALIS 
    euphrasia tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0360-0172
    Route of Administration SUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL) EUPHRASIA STRICTA 6 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    ACACIA (UNII: 5C5403N26O)  
    Product Characteristics
    Color white Score score with uneven pieces
    Shape ROUND Size 5mm
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0360-0172-01 1 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/17/1997
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 02/17/1997
    Labeler - STANDARD HOMEOPATHIC COMPANY (008316655)
    Establishment
    Name Address ID/FEI Business Operations
    STANDARD HOMEOPATHIC COMPANY 008316655 manufacture(0360-0172) , pack(0360-0172) , label(0360-0172)
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