Label: 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 March 8, 2024

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

  • INDICATIONS & USAGE

    Directions: FOR ORAL USE ONLY.

  • 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.

  • 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

  • INACTIVE INGREDIENT

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

  • PURPOSE

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

  • 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. 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
    shopuriel.com Lot:

  • PRINCIPAL DISPLAY PANEL

    Carbo Chamomilla Powder

  • INGREDIENTS AND APPEARANCE
    CARBO CHAMOMILLA 
    carbo chamomilla powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-3257
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GEUM URBANUM ROOT (UNII: 33P1Z2B61F) (GEUM URBANUM ROOT - UNII:33P1Z2B61F) GEUM URBANUM ROOT3 [hp_X]  in 1 g
    BLACK PEPPER (UNII: KM66971LVF) (BLACK PEPPER - UNII:KM66971LVF) BLACK PEPPER5 [hp_X]  in 1 g
    GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ) GINGER3 [hp_X]  in 1 g
    ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U) ANTIMONY TRISULFIDE4 [hp_X]  in 1 g
    ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE6 [hp_X]  in 1 g
    ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F) (ACORUS CALAMUS ROOT - UNII:XY1K7KIQ0F) ACORUS CALAMUS ROOT4 [hp_X]  in 1 g
    ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL2 [hp_X]  in 1 g
    WORMWOOD (UNII: F84709P2XV) (WORMWOOD - UNII:F84709P2XV) WORMWOOD3 [hp_X]  in 1 g
    MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ) MATRICARIA RECUTITA3 [hp_X]  in 1 g
    GENTIANA LUTEA ROOT (UNII: S72O3284MS) (GENTIANA LUTEA ROOT - UNII:S72O3284MS) GENTIANA LUTEA ROOT3 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    KAOLIN (UNII: 24H4NWX5CO)  
    ANISE OIL (UNII: 6Y89129C8H)  
    CARAWAY OIL (UNII: C2J9B08Q3I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-3257-460 g in 1 BOTTLE, GLASS; 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 Inc043471163manufacture(48951-3257)