Label: CVS ARNICA CREAM- arnica montana cream

  • 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 October 31, 2023

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

  • ACTIVE INGREDIENT

    Arnica Montana 1X HPUS-7%

  • PURPOSE

    Trauma, Muscle Pain and stiffness, swelling from injuries, discoloration from bruising.

    The letters HPUS indicate that this ingredient is officially included in the Homeopathic Pharmacopoeia of the United States.

  • INDICATIONS & USAGE

    temporarily relieves muscle pain and stiffness due to minor injuries, overexertion, and falls

    reduces pain, swelling and discoloration from bruises

  • WARNINGS

    For external use only

    Avoid contact with eyes, mucous membrane, damaged skin, or wounds.

  • DO NOT USE

    If you are allergic to Arnica montana or to any of this product's inactive ingredient.

  • WHEN USING

    Use only as directed.

    Do not bandage tightly or use a heating pad.

  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION

    Apply a thin layer of Arnica Cream to the affected area and massage gently as soon as possible after a minor injury, repeat 3 times a day or as needed.

  • OTHER SAFETY INFORMATION

    Store at 20-25 C (68-77 F)

    Do not use if the tube seal is broken

  • INACTIVE INGREDIENT

    Alcohol, Aloe Oil, Caprylic/Capric Triglycerides, Coconut oil, Helianthus Annus seed wax, and Sodium polyacrylate, Phenoxyethanol, Purified water, safflower oil, Shea butter.

  • QUESTIONS

    1-800-746-7287

  • PRINCIPAL DISPLAY PANEL

    Package Label

  • INGREDIENTS AND APPEARANCE
    CVS ARNICA CREAM 
    arnica montana cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51316-995
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA1 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SAFFLOWER OIL (UNII: 65UEH262IS)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
    ALCOHOL (UNII: 3K9958V90M)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)  
    ALOE (UNII: V5VD430YW9)  
    HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51316-995-251 in 1 BOX03/28/2022
    170 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic03/28/2022
    Labeler - CVS Health (062312574)