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![KALI TELLURICOSUM PELLET [HAHNEMANN LABORATORIES, INC.]](https://medic.hrt.org//dailymed/images/4eb5df53-43eb-0542-e054-00144ff8d46c/Kali-tell.jpg)
- PATIENT MEDICATION INFORMATION
- ACTIVE INGREDIENT
- DOSAGE FORMS & STRENGTHS
- INDICATIONS & USAGE
- PURPOSE
- DOSAGE & ADMINISTRATION
- ROUTE, METHOD AND FREQUENCY OF ADMINISTRATION
- WARNINGS
- WARNINGS AND PRECAUTIONS
- PREGNANCY OR BREAST FEEDING
- ASK DOCTOR
- INSTRUCTIONS FOR USE
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- QUESTIONS
- INACTIVE INGREDIENT
- Single label image contains content for sections 1-17.
-
INGREDIENTS AND APPEARANCE
KALI TELLURICOSUM
kali telluricosum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63545-681 Route of Administration ORAL, BUCCAL, SUBLINGUAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM TELLURITE (UNII: 71M41949N8) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM TELLURITE 30 [hp_C] in 1 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63545-681-01 240 [hp_C] in 1 VIAL, GLASS; Type 0: Not a Combination Product 05/04/2017 
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/04/2017 Labeler - Hahnemann Laboratories, Inc. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, Inc. 147098081 manufacture(63545-681)
