Label: ARGENTUM 0.4 ADULT SIZE- COCOA BUTTER SPECIAL ORDER suppository

  • 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 April 16, 2018

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

  • INDICATIONS & USAGE

    Directions: FOR RECTAL USE.

  • DOSAGE & ADMINISTRATION

    Insert 1 suppository as needed.

  • ACTIVE INGREDIENT

    Active Ingredient: 100 gm contains:
    4 gm Argentum met. (Silver) 1X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Cocoa butter, Micronized silica gel

  • PURPOSE

    Use: Temporary relief of headache.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • WARNINGS

    Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seals on box are broken or missing.

    KEEP REFRIGERATED OR STORE IN COOL, DRY PLACE.

    REFRIGERATE TO RESOLIDIFY.

  • QUESTIONS

    Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 www.urielpharmacy.com

  • PRINCIPAL DISPLAY PANEL

    Argentum0.4ADULTSOSuppository

  • INGREDIENTS AND APPEARANCE
    ARGENTUM 0.4 ADULT SIZE (COCOA BUTTER) SPECIAL ORDER 
    argentum 0.4 adult size (cocoa butter) special order suppository
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-1221
    Route of AdministrationRECTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER1 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    COCOA BUTTER (UNII: 512OYT1CRR)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-1221-110 in 1 BOX09/01/2009
    12 g in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/01/2009
    Labeler - Uriel Pharmacy Inc. (043471163)
    Establishment
    NameAddressID/FEIBusiness Operations
    Uriel Pharmacy Inc.043471163manufacture(48951-1221)