Label: POLLEN GUARD WEED MIX WEED POLLEN HAY FEVER SYMPTOM RELIEF- plantago lanceolata 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 September 27, 2011

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  • ACTIVE INGREDIENT


    English Plantain (Plantago lanceolata) 1X
  • PURPOSE

    Hay Fever Symptom Relief

  • INDICATIONS & USAGE

    temporarily relieves symptoms of hay fever resulting from exposure to weed pollen such as:

    • runny nose
    • nasal congestion/pressure
    • sneezing
    • itching
    • water, itchy eyes
    • hives
  • WARNINGS

    Do not use

    • if you have asthma, severe immunodeficiencies, malignancies, or autoimmune disease
    • if you take beta blockers
  • WHEN USING

    When using this product

    • avoid other drugs and medications
    • avoid food, drink, or teeth brushing for at least 5 minutes after each dose

  • STOP USE

    Stop use and ask a doctor if

    • condition persists or worsens
    • mouth, throat, chest or abdominal discomfort occurs
    • you experience hives, itching, or shortness of breath
  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast feeding, ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions

    • drop of extract may be placed under tongue, retained under the tongue for 2 minutes, then swallowed
    • adults: take 1 drop (0.05 mL) 2 or 3 times per day before meals
    • children over 3 years of age: only use treatment regimen if child has experienced more than 6 months of symptoms and is documented for allergies to weed pollen
    • children under 3 years of age: ask a doctor


  • STORAGE AND HANDLING

    • Store between 2-8 degrees C
    • Do not use if safety seal is broken
  • INACTIVE INGREDIENT

    Glycerin, Water

  • QUESTIONS

    Questions or Comments?

    1-866-335-5294 Monday through Friday 9am-5pm

  • PRINCIPAL DISPLAY PANEL

    Weed Mix Label

  • INGREDIENTS AND APPEARANCE
    POLLEN GUARD WEED MIX  WEED POLLEN HAY FEVER SYMPTOM RELIEF
    plantago lanceolata liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76097-004
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (PLANTAGO LANCEOLATA POLLEN - UNII:DO87T1U2CI) PLANTAGO LANCEOLATA POLLEN1 [hp_X]  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76097-004-055 mL in 1 BOTTLE, UNIT-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic10/03/2011
    Labeler - Western Allergy Services Ltd. (208003467)
    Registrant - Western Allergy Services Ltd. (208003467)
    Establishment
    NameAddressID/FEIBusiness Operations
    Quantum Allergy Canada, Inc.246829324manufacture
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