Label: 365 EVERYDAY VALUE ARNICA - arnica montana gel

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

Drug Label Information

Updated 05/15

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

  • WHEN USING

    Stop use and ask a doctor if condition persists for more than 3 days or worsens.

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  • STORAGE AND HANDLING

    Store at 68-77oF (20-25oC)

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  • INACTIVE INGREDIENT

    Alcohol, carbomer, dimethicone copolyol, purified water, sodium hydroxide

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  • QUESTIONS

    Whole Foods Market

    550 Bowie Street * Austin, TX 78703

    (c)2007 Whole Foods Market IP, LP

    Made in France

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  • ACTIVE INGREDIENT

    Arnica Montana 1X HPUS-7%  ---- Trauma, bruises, stiffness, muscle soreness

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  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

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  • INDICATIONS & USAGE

    For relief of muscle aches and stiffness due to minor injuries, ushc as strains, falls and blows. Reduces pain, swelling and discoloration from bruises.

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  • DOSAGE & ADMINISTRATION

    Apply a thin layer of Arnica Gel to affected area as soon as possible after minor injury. Repeat 3 times a day or as needed.

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  • WARNINGS

    For external use only

    Avoid contact with eyes and with open wounds. Do not use on broken skin.

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


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  • PRINCIPAL DISPLAY PANEL

    Arnica Gel Arnica Gel

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  • INGREDIENTS AND APPEARANCE
    365 EVERYDAY VALUE ARNICA 
    arnica montana gel
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:42681-0512
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 1 [hp_X]
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:42681-0512-5 1 in 1 BOX; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 09/01/2008
    Labeler - WFM Private Label, LP (196175616)
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