BARIUM CONCHAE- barium conchae liquid 
Uriel Pharmacy Inc.

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.

----------

Barium Conchae

Directions: FOR ORAL USE ONLY.

Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

Active Ingredients: Barium iodatum (Barium iodide) 4X, Berberis (Barberry) 4X, Cinnabar (Nat. mercuric sulfide) 6X, Ferrum arsenicosum (Nat. ferric arsenate) 6X, Barium citricum (Barium citrate) 8X, Conchae (Oyster shells) 10X

Inactive Ingredients: Distilled water, Organic cane alcohol, Lactose

Use: Temporary relief of sore throat.

KEEP OUT OF REACH OF CHILDREN.

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

barconliq

BARIUM CONCHAE 
barium conchae liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-2026
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MERCURIC SULFIDE (UNII: ZI0T668SF1) (MERCURIC CATION - UNII:ED30FJ8Y42) MERCURIC SULFIDE6 [hp_X]  in 1 mL
BARIUM CITRATE (UNII: J9X0Y34WC2) (BARIUM CATION - UNII:V645272HLN) BARIUM CITRATE8 [hp_X]  in 1 mL
BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK4 [hp_X]  in 1 mL
FERROUS ARSENATE (UNII: 129CO35H12) (FERROUS ARSENATE - UNII:129CO35H12) FERROUS ARSENATE6 [hp_X]  in 1 mL
OSTREA EDULIS SHELL (UNII: 49OY13BE7Z) (OSTREA EDULIS SHELL - UNII:49OY13BE7Z) OSTREA EDULIS SHELL10 [hp_X]  in 1 mL
BARIUM IODATE (UNII: ST2993NJ5J) (BARIUM IODATE - UNII:ST2993NJ5J) BARIUM IODATE4 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
LACTOSE (UNII: J2B2A4N98G)  
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-2026-31 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(48951-2026)

Revised: 8/2017
Document Id: 56e16db3-dbba-494c-e054-00144ff8d46c
Set id: 34a0b4ee-747e-4ca0-af89-80b232172efe
Version: 4
Effective Time: 20170816
 
Uriel Pharmacy Inc.