ARNICA PC - arnica montana root tablet 
Heel Inc

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.

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Arnica PC Tablet

KEEP OUT OF REACH OF CHILDREN

    Keep this and all medicines out of the reach of children.

INDICATIONS AND USAGE

For the temporary relief of:

  • Muscle Injury
  • Metal Stress or Shock
  • General Exhaustion


WARNINGS

If symptoms persist or worsen, a physician should be consulted. As with any drug, if you are pregnant or nursing a baby, seek the advice of a health care professional before using this product.

DOSAGE AND ADMINISTRATION

Adults and children above 6 years: 1 tablet sublingually or dissolved completely in mouth 3 times daily or as directed by a physician. Infants and children to 6 years: 1/2 the adult dosage.

ACTIVE INGREDIENT

Each 300 mg tablet contains as active ingredients: Arnica montana radix 6X, 12X, 30X, 200X 75 mg each.

INACTIVE INGREDIENT

    Lactose, Magnesium stearate

PURPOSE

 Muscle Injury, Metal Stress or Shock, General Exhaustion


Arnica PC Tablet.jpg


ARNICA PC 
arnica montana root tablet
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:50114-2316
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ARNICA MONTANA ROOT (ARNICA MONTANA ROOT) ARNICA MONTANA ROOT6 [hp_X]  in 300 mg
Inactive Ingredients
Ingredient NameStrength
LACTOSE 
MAGNESIUM STEARATE 
Product Characteristics
ColorwhiteScoreno score
ShapeROUND (Tablet) Size9mm
FlavorImprint Code BHI;O;M
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50114-2316-230000 mg in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic01/31/2000
Labeler - Heel Inc (102783016)
Establishment
NameAddressID/FEIBusiness Operations
Heel Inc102783016manufacture

Revised: 4/2012
Document Id: dbd5383f-a51a-4ded-b3e4-b120405dca4f
Set id: 87965d9c-237c-46ce-835b-43888f47a4a3
Version: 1
Effective Time: 20120405
 
Heel Inc