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- 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
RUBIDIUM FLUORATUM
rubidium fluoratum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63545-673 Route of Administration BUCCAL, SUBLINGUAL, ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUBIDIUM FLUORIDE (UNII: 63564TNJ4R) (RUBIDIUM FLUORIDE - UNII:63564TNJ4R) RUBIDIUM FLUORIDE 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:63545-673-01 240 [hp_C] in 1 VIAL, GLASS; Type 0: Not a Combination Product 12/01/2016 
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/01/2016 Labeler - Hahnemann Laboratories, Inc. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, Inc. 147098081 manufacture(63545-673)
