Label: THYMUS VULGARIS (N)- thyme tincture

  • 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 23, 2018

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  • Use

    For temporary relief of asthma and spastic cough

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  • Directions

    Adults and children above 12 years: 2-5 drops 1-3 times daily in pure water before meals. Consult a physician for use in children under 12 years of age.

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  • Ingredients

    Thymus vulgaris Ø (N)

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  • INACTIVE INGREDIENT

    Alcohol: 65

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  • TAMPER-EVIDENT

    Do not use if tamper evident strip is broken from base of cap.

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  • WARNING

    Ask a doctor if you are pregnant or nursing.

    Keep away from children. In case of overdose, call a medical professional.

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  • PRINCIPAL DISPLAY PANEL - 20 ml Bottle Label

    CERES®
    Homeopathic Medicine

    Thymus vulgaris Ø (N)

    Use: For temporay relief of asthma and spastic cough

    Directions : Adults and children above 12 years: 2-5
    drops 1-3 times daily in pure water before meals. Consult
    a physician for use in children under 12 years of age.

    0.67 fl.oz. (20ml)
    Lot#:1234567A
    EXP: 99.9999

    Principal Display Panel - 20 ml Bottle Label
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  • INGREDIENTS AND APPEARANCE
    THYMUS VULGARIS (N) 
    thyme tincture
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:13838-1447
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    THYME (UNII: CW657OBU4N) (THYME - UNII:CW657OBU4N) THYME 1 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    ALCOHOL (UNII: 3K9958V90M)  
    Product Characteristics
    Color BROWN Score     
    Shape Size
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:13838-1447-1 20 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/01/2005
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    UNAPPROVED HOMEOPATHIC 10/01/2005
    Labeler - Phytodyne Inc. (164980927)
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