Label: CUPRUM METALLICUM 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 January 20, 2020

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

View All Sections
  • ACTIVE INGREDIENT

    Cuprum Metallicum 6X, HPUS

  • PURPOSE

    Enter section text here

  • Uses:

    For temporary relief of venous congestion and muscle spasms. May also be used for standard homeopathic indications or as directed by your physician.

  • Warnings:

    For external use only. Do not apply on open wounds, damaged skin or eyes. Consult your health care provider if symptoms persist more than 5 days or worsen or rash occurs.

  • PREGNANCY OR BREAST FEEDING

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children.

  • DO NOT USE

    TAMPER EVIDENT: Do not use if safety seal is broken before first use.

  • Directions for Use:

    Adults, children and infants: Apply to desired area 3-4 times daily. Rub in thoroughly until cream is absorbed.

  • Other Ingredients:

    Almond Oil, Beeswax, Citric Acid, Glycerine, Jojoba Oil, Kokum Butter, Lavendar Essential Oil, Plant Emulsifiers, Potassium Sorbate, Vitamin E, Water.

  • QUESTIONS



    Developed and Made by

    True Botanica, LLC

    1005 Richards Rd., Suite D

    Hartland, WI 53029

    800-315-8783

    www.truebotanica.com

  • Cuprum Cream

    Display Panel

  • INGREDIENTS AND APPEARANCE
    CUPRUM METALLICUM 
    cuprum metallicum cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53645-1050
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER6 [hp_X]  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALMOND OIL (UNII: 66YXD4DKO9)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    JOJOBA OIL (UNII: 724GKU717M)  
    GARCINIA INDICA SEED BUTTER (UNII: US2H3D7800)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53645-1050-150 mL in 1 JAR; Type 0: Not a Combination Product02/27/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic02/27/2013
    Labeler - True Botanica, LLC (182071519)
    Establishment
    NameAddressID/FEIBusiness Operations
    True Botanica, LLC182071519manufacture(53645-1050)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!