Label: EQUISETUM CUM SULFURE TOSTA 6 powder

  • 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 November 17, 2023

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  • INDICATIONS & USAGE

    Directions: FOR ORAL USE ONLY

  • DOSAGE & ADMINISTRATION

    Take 3-4 times daily. Ages 12 and older:
    1/8 teaspoon. Ages 2-11: 1/16 teaspoon.

  • ACTIVE INGREDIENT

    Active Ingredient: Equisetum cum Sulfure tosta (Equisetum, Sulfur) 6X

  • INACTIVE INGREDIENT

    Inactive Ingredient: Lactose

  • PURPOSE

    Use: Temporary relief of urinary irritation.

  • 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. Contains lactose. 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 seal is broken or missing.

  • QUESTIONS

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

  • PRINCIPAL DISPLAY PANEL

    Equisetum cum Sulfure tosta 6X Powder

  • INGREDIENTS AND APPEARANCE
    EQUISETUM CUM SULFURE TOSTA 6 
    equisetum cum sulfure tosta 6 powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-4060
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (EQUISETUM ARVENSE TOP - UNII:1DP6Y6B65Z) EQUISETUM ARVENSE TOP6 [hp_X]
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR6 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE (UNII: J2B2A4N98G)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-4060-71 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product09/01/2009
    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(48951-4060)
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