Label: CICHORIUM OXALIS liquid

  • Category: HUMAN OTC 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 February 2, 2024

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

View All Sections
  • 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: Cichorium (Wild chicory) 3X, Oxalis (Wood sorrel) 3X, Carbo Betulae (Birch wood charcoal) 6X, Pancreas (Bovine pancreas) 6X, Barium citricum (Barium citrate) 10X, Ferrum sidereum (Meteoric iron) 20X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, Salt, Lactose

    "prepared using rhythmical processes"

  • PURPOSE

    Use: Temporary relief of headache.

  • 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 Made by Uriel, East Troy, WI 53120 shopuriel.com Lot:

  • PRINCIPAL DISPLAY PANEL

    Cichorium Oxalis Ampules

  • INGREDIENTS AND APPEARANCE
    CICHORIUM OXALIS 
    cichorium oxalis liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-3091
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CICHORIUM INTYBUS WHOLE (UNII: 1KE45XD28S) (CICHORIUM INTYBUS WHOLE - UNII:1KE45XD28S) CICHORIUM INTYBUS WHOLE3 [hp_X]  in 1 mL
    OXALIS ACETOSELLA LEAF (UNII: U1W3U02EW0) (OXALIS ACETOSELLA LEAF - UNII:U1W3U02EW0) OXALIS ACETOSELLA LEAF3 [hp_X]  in 1 mL
    ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL6 [hp_X]  in 1 mL
    SUS SCROFA PANCREAS (UNII: 9Y3J3362RY) (SUS SCROFA PANCREAS - UNII:9Y3J3362RY) SUS SCROFA PANCREAS6 [hp_X]  in 1 mL
    BARIUM CITRATE (UNII: J9X0Y34WC2) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) BARIUM CITRATE10 [hp_X]  in 1 mL
    IRON (UNII: E1UOL152H7) (IRON - UNII:E1UOL152H7) IRON20 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-3091-110 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(48951-3091)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!