Label: ARNICA MONTANA 30C- arnica montana pellet

  • NDC Code(s): 61727-111-75
  • 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 March 20, 2019

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

  • Active Ingredients:

    (HPUS) Arnica Montana 30C

  • Purpose:

    Helps reduce bruising, swelling and pain associated with injuries, trauma, surgical procedures and arthritis.

  • Indications & Usage:

    Helps reduce bruising, swelling, and pain associated with injuries, trauma, surgical procedures, and arthritis.

  • Warnings:

    If symptoms persist or worsen, or if nursing, consult a doctor. Keep out of reach of children. Do not use if cap seal is broken or missing.

  • Keep out of reach of children.

    Keep out of reach of children.

  • Inactive Ingredients:

    Sucrose/lactose.

  • Dosage & Administration:

    Turn tube upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to dissolve under your tongue 3 times a day or as needed. Take apart from food or drinks. To preserve purity avoid touching pellets with fingers.

  • Arnica Montana 30C

    ArnicaMontana30C Label.jpg

  • INGREDIENTS AND APPEARANCE
    ARNICA MONTANA 30C 
    arnica montana pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61727-111
    Route of AdministrationSUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA30 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    LACTOSE (UNII: J2B2A4N98G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61727-111-7580 in 1 TUBE; Type 0: Not a Combination Product06/11/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/11/2012
    Labeler - Homeocare Laboratories (088248828)
    Registrant - Homeocare Laboratories (088248828)
    Establishment
    NameAddressID/FEIBusiness Operations
    Homeocare Laboratories088248828manufacture(61727-111)