Label: HEPAR SULFURIS SINUS liquid

  • Category: HUMAN PRESCRIPTION DRUG LABEL

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 2, 2014

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • INDICATIONS & USAGE

    Directions: FOR ORAL USE ONLY.

  • DOSAGE & ADMINISTRATION

    Take the contents of one ampule
    under the tongue and hold for
    30 seconds, then swallow.

  • ACTIVE INGREDIENT

    Active Ingredients: Hepar sulfuris 6X, Membrana sinus frontalis 8X,
    Membrana sinus maxillaris 8X,
    Membrana sinus sphenoidalis 8X,
    Membrana sinuum paranasalium 8X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, Salt, Lactose

  • PURPOSE

    Use: Temporary relief of sinus congestion.

  • KEEP OUT OF REACH OF CHILDREN


    KEEP OUT OF REACH OF CHILDREN.

  • WARNINGS

    Warnings: Do not use if allergic to any ingredient. Consult a doctor before use if lactose intolerant. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Natural ingredients may cause color, scent and/or taste variation.

  • QUESTIONS

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

  • PRINCIPAL DISPLAY PANEL

    product label

  • INGREDIENTS AND APPEARANCE
    HEPAR SULFURIS SINUS 
    hepar sulfuris sinus liquid
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:48951-5049
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE6 [hp_X]  in 1 mL
    BOS TAURUS NASAL MUCOSA (UNII: 343455G79K) (BOS TAURUS NASAL MUCOSA - UNII:343455G79K) BOS TAURUS NASAL MUCOSA8 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    LACTOSE (UNII: J2B2A4N98G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-5049-110 in 1 BOX
    11 mL in 1 AMPULE
    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(48951-5049)