Label: ARGENTUM METALLICUM 30X liquid

  • 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 9, 2024

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

View All Sections
  • ACTIVE INGREDIENT

    Argentum Metallicum 30X

  • PURPOSE

    For temporary relief of cramps in reproductive area. Supports illness recovery. May also be used for standard homeopathic indications or as directed by your physician.

  • Use:

    For temporary relief of cramps in reproductive area. Supports illness recovery. May also be used for standard homeopathic indications or as directed by your physician.

  • Warnings:

    Consult your health care provider if symptoms persist more than 5 days or worsen.

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breastfeeding ask a health professional before use.

  • 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:

    Place drops under tongue for 30 seconds. Adults 7 drops 3 times a day. Children 2-12 years, 7 drops 3 times a day. Under 2 years, consult your doctor. Use until symptoms are relieved or as directed by your health care provider.

  • Other Ingredients:

    Citric Acid, Potassium Sorbate, Water

  • QUESTIONS

    Developed and Made by

    True Botanica, LLC

    1005 Richards Rd., Suite D

    Hartland, WI 53029

    800-315-8783

    www.truebotanica.com

  • Principal Display Panel

    Argentum Metallicum 30X_30ml_V1

  • INGREDIENTS AND APPEARANCE
    ARGENTUM METALLICUM 30X 
    argentum metallicum 30x liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53645-1033
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER30 [hp_X]  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53645-1033-630 mL in 1 BOTTLE; Type 0: Not a Combination Product12/09/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic12/09/2024
    Labeler - True Botanica, LLC (182071519)
    Establishment
    NameAddressID/FEIBusiness Operations
    True Botanica, LLC182071519manufacture(53645-1033)
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!