LYSIMACHIA SOLANUM SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]

LYSIMACHIA SOLANUM SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]
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NDC 48951-6052-1
Set ID fc9645a9-ccda-49ea-a0e3-994f12953396
Category HUMAN OTC DRUG LABEL
Packager Uriel Pharmacy Inc.
Generic Name
Product Class
Product Number
Application Number
  • INDICATIONS & USAGE

    Directions: FOR ORAL USE.

  • DOSAGE & ADMINISTRATION

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

  • ACTIVE INGREDIENT

    Active Ingredients: 100 gm contains: 2.5 gm Lysimachia nummularia (Pennywort) 1X, 2.5 gm Solanum dulcamara (Bittersweet nightshade) 1X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, Salt

  • PURPOSE

    Use: Temporary relief of skin rash.

  • 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.

  • QUESTIONS

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

  • PRINCIPAL DISPLAY PANEL

    LysimachiaSolanumSOAmpules

  • INGREDIENTS AND APPEARANCE
    LYSIMACHIA SOLANUM SPECIAL ORDER 
    lysimachia solanum special order liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-6052
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LYSIMACHIA NUMMULARIA (UNII: H13E98RT77) (LYSIMACHIA NUMMULARIA - UNII:H13E98RT77) LYSIMACHIA NUMMULARIA1 [hp_X]  in 1 mL
    SOLANUM DULCAMARA FLOWER (UNII: W6J1279A6K) (SOLANUM DULCAMARA FLOWER - UNII:W6J1279A6K) SOLANUM DULCAMARA FLOWER1 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-6052-110 in 1 BOX09/01/2009
    11 mL in 1 AMPULE; Type 1: Convenience Kit of Co-Package
    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(48951-6052)

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