Label: ARNICA RELIEF- arnica montana 30c tablet tablet

  • NDC Code(s): 61727-111-10
  • Packager: Homeocare Laboratories
  • 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 21, 2018

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  • Active Ingredients:

    Arnica Montana 30C

  • Inactive Ingredients:

    Lactose, Magnesium Stearate

  • Purpose:

    For relief of pain, bruises, muscle aches, injuries, and pre and post surgery.

  • Keep out of reach of children.

    Keep out of reach of children.

  • Indications & Usage:

    Slightly chew one tablet and allow to dissolve in the mouth, 3 times a day. For best results avoid eating at least 15 minutes before or after taking the remedy.

  • Warnings:

    If pregnant, breast-feeding or symptoms persist or worsen, discontinue use and consult a physician. Keep out of reach of children. Do not use if inner seal is broken or missing.

  • Dosage & Administration:

    Slightly chew one tablet and allow to dissolve in the mouth, 3 times a day. For best results avoid eating at least 15 minutes before or after taking the remedy.

  • Arnica Relief Tablets



    Arnica Montana 100 Tabs.jpg

  • INGREDIENTS AND APPEARANCE
    ARNICA RELIEF 
    arnica montana 30c tablet tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61727-111
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA30 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE (UNII: J2B2A4N98G)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    ColorwhiteScore2 pieces
    ShapeROUNDSize10mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61727-111-10100 in 1 BOTTLE; Type 0: Not a Combination Product07/06/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/06/2012
    Labeler - Homeocare Laboratories (088248828)
    Registrant - Homeocare Laboratories (088248828)
    Establishment
    NameAddressID/FEIBusiness Operations
    Homeocare Laboratories088248828manufacture(61727-111)
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