Label: NATURASIL INTERNAL PARASITES- sulfur liquid

  • NDC Code(s): 10893-270-30
  • Packager: Nature's Innovation, Inc.
  • 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 14, 2021

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

  • ACTIVE INGREDIENT

    Drug Facts

    Active Ingredients:

    Sulfur 6X HPUS

  • DESCRIPTION

    The letters HPUS indicate that the component(s) in this product is (are) officially

    Monographed in the Homeopathic Pharmacopeia of the United States. 

  • PURPOSE

    Purpose

    Internal Parasite Symptom Relief

  • INDICATIONS & USAGE

    Uses:  Symptomatic treatment of internal parasites.

  • WARNINGS

    Warnings:

    Do Not use this product if pregnant or nursing, or children under the age of seven (7) years of age.

    If eye contact occurs, rinse thoroughly with water.

    Keep out of reach of children.

    Do not use if tamper evident seal is broken.

  • DOSAGE & ADMINISTRATION

    Directions: Shake Well! Take 1/2 to 2 droppers full with juice 2 to 3 times daily for two weeks. Take a one week break before repeating.

  • INACTIVE INGREDIENT

    Inactive Ingredients:  Black Walnut Tincture in Ethyl Alcohol (Juglans Nigra), Clove Bud Extract Tincture in Ethyl Alcohol (Caryophyllus Aromaticus).

  • QUESTIONS

    Questions? www.naturasil.com 1-866-371-2499

    Mfd. by: Nature's Innovation, Inc.

    2723 Brickton North Dr., Buford, GA 30518

  • PRINCIPAL DISPLAY PANEL

    100%

    Natural Plant

    Extracts

    Naturasil

    30ml (1.014 fl. oz.)
    Liquid
    Homeopathic Medicine
    Internal Parasites

    Internal Parasites Label

  • INGREDIENTS AND APPEARANCE
    NATURASIL  INTERNAL PARASITES
    sulfur liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10893-270
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR6 [hp_X]  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    BLACK WALNUT (UNII: 02WM57RXZJ)  
    ALCOHOL (UNII: 3K9958V90M)  
    CLOVE (UNII: K48IKT5321)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10893-270-3030 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product01/11/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic01/11/2012
    Labeler - Nature's Innovation, Inc. (602969854)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nature's Innovation, Inc.602969854manufacture(10893-270)