Label: CARBO CHAMOMILLA- carbo chamomilla powder

  • 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 April 24, 2018

If you are a consumer or patient please visit this version.

  • INDICATIONS & USAGE

    Directions: FOR ORAL USE ONLY.

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  • DOSAGE & ADMINISTRATION

    Take 3-4 times daily. Ages 12 and older: Mix 1/4 teaspoon with water. Ages 2-11: Mix 1/8 teaspoon with water. Under age 2: Consult a doctor.

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  • ACTIVE INGREDIENT

    Active Ingredients: Carbo betulae (Birch wood charcoal) 2X, Absinthium (Wormwood) 3X, Chamomilla (Chamomile) 3X, Gentiana (Yellow gentian) 3X, Geum urb. (Herb bennet) 3X, Zingiberis (Ginger) 3X, Antimonite (Nat. antimony trisulfide) 4X, Calamus (Sweet flag) 4X, Piper nig. (Black pepper) 5X Arsenicum album (White arsenic) 6X

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  • INACTIVE INGREDIENT

    Inactive Ingredients: Kaolin, Anise oil, Caraway oil, Lactose

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  • PURPOSE

    Uses: Temporarily relieves symptoms of upset stomach, diarrhea and flatulence.

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  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

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  • WARNINGS

    Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains lactose. 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.

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  • QUESTIONS


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

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  • INGREDIENTS AND APPEARANCE
    CARBO CHAMOMILLA 
    carbo chamomilla powder
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-3206
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL 2 [hp_X]
    WORMWOOD (UNII: F84709P2XV) (WORMWOOD - UNII:F84709P2XV) WORMWOOD 3 [hp_X]
    MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ) MATRICARIA RECUTITA 3 [hp_X]
    GENTIANA LUTEA ROOT (UNII: S72O3284MS) (GENTIANA LUTEA ROOT - UNII:S72O3284MS) GENTIANA LUTEA ROOT 3 [hp_X]
    AVENS EXTRACT (UNII: Q2GJW5TP2C) (AVENS EXTRACT - UNII:Q2GJW5TP2C) AVENS EXTRACT 3 [hp_X]
    BLACK PEPPER (UNII: KM66971LVF) (BLACK PEPPER - UNII:KM66971LVF) BLACK PEPPER 3 [hp_X]
    GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ) GINGER 3 [hp_X]
    ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY TRISULFIDE 3 [hp_X]
    ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE 6 [hp_X]
    Inactive Ingredients
    Ingredient Name Strength
    KAOLIN (UNII: 24H4NWX5CO)  
    ANISE OIL (UNII: 6Y89129C8H)  
    CARAWAY OIL (UNII: C2J9B08Q3I)  
    ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:48951-3206-7 1 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/01/2009
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 09/01/2009
    Labeler - Uriel Pharmacy Inc (043471163)
    Establishment
    Name Address ID/FEI Business Operations
    Uriel Pharmacy Inc 043471163 manufacture(48951-3206)
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