CARBO CHAMOMILLA capsule

Carbo Chamomilla by

Drug Labeling and Warnings

Carbo Chamomilla by is a Homeopathic medication manufactured, distributed, or labeled by Uriel Pharmacy Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION

Ages 12 and older: 1-2 capsules 3-4 times daily. Ages 2-11: 1 capsule 3-4 times daily. Under age 2: Consult a doctor.

ACTIVE INGREDIENT

Active Ingredients: Antimonite (Nat. antimony trisulfide) 3X, Chamomilla e rad. (Chamomile) 3X, Geum urbanum e rad. (Herb bennet) 3X, Absinthium ex herba (Wormwood) 5X, Gentiana e rad. (Yellow gentian) 5X, Zingiberis e rhiz. (Ginger) 5X, Arsenicum album (White arsenic) 6X, Calamus e rhiz. (Sweet flag) 6X, Piper nig. e fruct. (Black pepper) 7X

INACTIVE INGREDIENT

Inactive Ingredients: Carbo Fagi, Vegetable capsules, Anise oil, Caraway oil

PURPOSE

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

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

WARNINGS

Allergen Statement: This product was produced on equipment that also processes products that contain lactose.

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

INGREDIENTS AND APPEARANCE

CARBO CHAMOMILLA 
carbo chamomilla capsule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 48951-3216
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F) (ACORUS CALAMUS ROOT - UNII:XY1K7KIQ0F)	ACORUS CALAMUS ROOT	6 [hp_X]
ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U)	ANTIMONY TRISULFIDE	3 [hp_X]
MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ)	MATRICARIA RECUTITA	3 [hp_X]
WORMWOOD (UNII: F84709P2XV) (WORMWOOD - UNII:F84709P2XV)	WORMWOOD	5 [hp_X]
GENTIANA LUTEA ROOT (UNII: S72O3284MS) (GENTIANA LUTEA ROOT - UNII:S72O3284MS)	GENTIANA LUTEA ROOT	5 [hp_X]
GEUM URBANUM ROOT (UNII: 33P1Z2B61F) (GEUM URBANUM ROOT - UNII:33P1Z2B61F)	GEUM URBANUM ROOT	3 [hp_X]
GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ)	GINGER	5 [hp_X]
BLACK PEPPER (UNII: KM66971LVF) (BLACK PEPPER - UNII:KM66971LVF)	BLACK PEPPER	7 [hp_X]
ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV)	ARSENIC TRIOXIDE	6 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
CARAWAY OIL (UNII: C2J9B08Q3I)
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
ANISE OIL (UNII: 6Y89129C8H)

Product Characteristics
Color	black	Score	no score
Shape	CAPSULE	Size	8mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48951-3216-7	90 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(48951-3216)