Label: BRYOPHYLLUM CONCHAE liquid

  • 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 December 17, 2024

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  • 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: Bryophyllum (Life plant) 5X, Conchae (Oyster shells) 7X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, Salt, Lactose

    Prepared using rhythmical processes.

  • PURPOSE

    Use: Temporary relief of sleeplessness.

  • 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 traces of lactose. 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 shopuriel.com Lot:

  • PRINCIPAL DISPLAY PANEL

    Bryophyllum Conchae Ampules

  • INGREDIENTS AND APPEARANCE
    BRYOPHYLLUM CONCHAE 
    bryophyllum conchae liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-2150
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    KALANCHOE DAIGREMONTIANA LEAF (UNII: L6X13JKL8O) (KALANCHOE DAIGREMONTIANA LEAF - UNII:L6X13JKL8O) KALANCHOE DAIGREMONTIANA LEAF5 [hp_X]  in 1 mL
    OSTREA EDULIS SHELL (UNII: 49OY13BE7Z) (OSTREA EDULIS SHELL - UNII:49OY13BE7Z) OSTREA EDULIS SHELL7 [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:48951-2150-110 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(48951-2150)
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