MEDULLA OSSIS SUIS- sus scrofa bone marrow pellet
MEDULLA OSSIS SUIS by
Drug Labeling and Warnings
MEDULLA OSSIS SUIS by is a Homeopathic medication manufactured, distributed, or labeled by BOIRON, BOIRON, INC.. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- SPL UNCLASSIFIED SECTION
- INACTIVE INGREDIENT
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MEDULLA OSSIS SUIS
sus scrofa bone marrow pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 0220-3329 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SUS SCROFA BONE MARROW (UNII: VP2CN2G7Y8) (SUS SCROFA BONE MARROW - UNII:VP2CN2G7Y8) SUS SCROFA BONE MARROW 8 [hp_X] in 8 [hp_X] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) 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: 0220-3329-41 8 [hp_X] in 1 TUBE; Type 0: Not a Combination Product 01/08/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/08/2018 Labeler - BOIRON (282560473) Registrant - BOIRON, INC. (014892269) Establishment Name Address ID/FEI Business Operations BOIRON 282560473 manufacture(0220-3329) Establishment Name Address ID/FEI Business Operations BOIRON 380022322 manufacture(0220-3329)
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