PULMO MERCURIUS SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]

PULMO MERCURIUS SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]
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NDC 48951-8229-3
Set ID 90ad66cf-eabe-4b29-8897-2fb1d74f96ea
Category HUMAN OTC DRUG LABEL
Packager Uriel Pharmacy Inc.
Generic Name
Product Class
Product Number
Application Number
  • INDICATIONS & USAGE

    Directions: FOR ORAL USE ONLY.

  • DOSAGE & ADMINISTRATION

    Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

  • ACTIVE INGREDIENT

    Active Ingredients: Pulmo (Bovine lung) 8X, Mercurius vivus (Mercury) 17X

  • INACTIVE INGREDIENT

    Inactive Ingredient: Distilled water

  • PURPOSE

    Use: Temporary relief of cough.

  • 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 seal is broken or missing.

    REFRIGERATE AFTER OPENING.
    BEST WHEN USED WITHIN 90 DAYS OF OPENING.

  • QUESTIONS

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

  • PRINCIPAL DISPLAY PANEL

    PulmoMercuriusSOLiquid

  • INGREDIENTS AND APPEARANCE
    PULMO MERCURIUS SPECIAL ORDER 
    pulmo mercurius special order liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-8229
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SUS SCROFA LUNG (UNII: 7GL3G1COB3) (SUS SCROFA LUNG - UNII:7GL3G1COB3) SUS SCROFA LUNG8 [hp_X]  in 1 mL
    MERCURY (UNII: FXS1BY2PGL) (MERCURY - UNII:FXS1BY2PGL) MERCURY17 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-8229-360 mL in 1 BOTTLE, DROPPER; 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(48951-8229)

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