Label: CEREBELLUM THALAMUS A liquid
- NDC Code(s): 48951-3048-1
- Packager: Uriel Pharmacy Inc.
- Category: HUMAN OTC 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.
Drug Label Information
Updated January 16, 2024
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- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
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ACTIVE INGREDIENT
Active Ingredients: Cerebellum (Bovine cerebellum) 8X, Chrysolith (Silicate of magnesium and iron) 8X, Corpora quadrig. (Bovine quad. plate) 8X, Gl. Thalamus (Bovine thymus gland) 8X, Hypophysis (Bovine pituitary gland) 8X, Iris (Bovine iris) 8X, Medula oblongata (Bovine myelencephalon) 8X, Nervus opticus (Porcine second cranial nerve) 8X, Retina et chorioidea (Bovine retina and choroid) 8X
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- WARNINGS
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CEREBELLUM THALAMUS A
cerebellum thalamus a liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-3048 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BOS TAURUS CEREBELLUM (UNII: Q09851U44F) (BOS TAURUS CEREBELLUM - UNII:Q09851U44F) BOS TAURUS CEREBELLUM 8 [hp_X] in 1 mL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 8 [hp_X] in 1 mL BOS TAURUS BRAIN (UNII: A1YEE2DB8Z) (BOS TAURUS BRAIN - UNII:A1YEE2DB8Z) BOS TAURUS BRAIN 8 [hp_X] in 1 mL SUS SCROFA THALAMUS (UNII: 3D6Q7UV74J) (SUS SCROFA THALAMUS - UNII:3D6Q7UV74J) SUS SCROFA THALAMUS 8 [hp_X] in 1 mL BOS TAURUS PITUITARY GLAND (UNII: 7JM57I419K) (BOS TAURUS PITUITARY GLAND - UNII:7JM57I419K) BOS TAURUS PITUITARY GLAND 8 [hp_X] in 1 mL BOS TAURUS EYE (UNII: VTW461N43P) (BOS TAURUS EYE - UNII:VTW461N43P) BOS TAURUS EYE 8 [hp_X] in 1 mL BOS TAURUS NERVE (UNII: 28G2U3MQJK) (BOS TAURUS NERVE - UNII:28G2U3MQJK) BOS TAURUS NERVE 8 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-3048-1 10 in 1 BOX 09/01/2009 1 1 mL in 1 AMPULE; Type 1: Convenience Kit of Co-Package Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/01/2009 Labeler - Uriel Pharmacy Inc. (043471163) Establishment Name Address ID/FEI Business Operations Uriel Pharmacy Inc. 043471163 manufacture(48951-3048)