CALCIUM CARB. CORTEX QUERCUS 30 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]

CALCIUM CARB. CORTEX QUERCUS 30 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]
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NDC 48951-3006-3
Set ID 292b838d-575d-4983-8b43-816277fe5190
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: Calcium carb. 30X, Cortex Quercus 30X

  • INACTIVE INGREDIENT

    Inactive Ingredient: Distilled water

  • 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. 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.

  • QUESTIONS

    Questions? Call 866.642.2858 Made with care by Uriel, East Troy, WI 53120 www.urielpharmacy.com

  • PRINCIPAL DISPLAY PANEL

    Calcium Carb. Cortex Quercus 30 s.o. Liquid

  • INGREDIENTS AND APPEARANCE
    CALCIUM CARB. CORTEX QUERCUS 30 SPECIAL ORDER 
    calcium carb. cortex quercus 30 special order liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-3006
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARBONATE ION (UNII: 7UJQ5OPE7D) (CARBONATE ION - UNII:7UJQ5OPE7D) CARBONATE ION30 [hp_X]  in 1 mL
    QUERCUS ROBUR WHOLE (UNII: R7QMG0BT2W) (QUERCUS ROBUR WHOLE - UNII:R7QMG0BT2W) QUERCUS ROBUR WHOLE30 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-3006-360 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(48951-3006)

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