Label: THALLIUM METALLICUM- thallium pellet
- NDC Code(s): 0220-4970-41
- Packager: Boiron
- Category: HUMAN PRESCRIPTION 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.
Updated April 26, 2019
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- ACTIVE INGREDIENT
Thallium metallicum 9C
(**contains 0.443 mg of the active ingredient per pellet)Close
- INDICATIONS & USAGE
- STOP USE
Stop use and ask a doctor if symptoms persist for more than 3 days or worsenClose
- PREGNANCY OR BREAST FEEDING
If pregnant or breast-feeding ask a health professional before useClose
- KEEP OUT OF REACH OF CHILDREN
Keep out of reach of childrenClose
- SPL UNCLASSIFIED SECTION
Do not use if pellet dispenser seal is broken.Close
Contains approx 80 pellets.
How to dispense pellets? Turn tube upside down. Twist until 5 pellets are dispensed into cap. Carefully remove the cap and use it to pour pellets under the tongue.
*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
*C,K,CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.
- INACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.Close
Distributed by Boiron, Inc. Newtown Square, PA 19073
- INGREDIENTS AND APPEARANCE
Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0220-4970 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength THALLIUM (UNII: AD84R52XLF) (THALLIUM - UNII:AD84R52XLF) THALLIUM 9 [hp_C] in 9 [hp_C] Inactive Ingredients Ingredient Name Strength LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score Shape ROUND Size 4mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0220-4970-41 9 [hp_C] in 1 TUBE; Type 0: Not a Combination Product 03/03/1983 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/03/1983 Labeler - Boiron (282560473) Registrant - Boiron, Inc. (014892269) Establishment Name Address ID/FEI Business Operations Boiron 282560473 manufacture(0220-4970)