Label: ARSENICUM CEREBRUM liquid
- NDC Code(s): 48951-1163-1
- 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 May 17, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
-
ACTIVE INGREDIENT
Active Ingredients: Arnica 6X, Lobus frontalis (Bovine frontal lobe of the brain) 8X, Lobus occipitalis (Bovine occipital lobe of the brain) 8X, Lobus parietalis (Bovine parietal lobe of the brain) 8X, Lobus temporalis (Bovine temporal lobe of the brain) 8X, Dyscrasite (Antimony silver sulfide) 20X, Arsenicum alb. (White arsenic) 30X
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- WARNINGS
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ARSENICUM CEREBRUM
arsenicum cerebrum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-1163 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARNICA MONTANA ROOT (UNII: MUE8Y11327) (ARNICA MONTANA ROOT - UNII:MUE8Y11327) ARNICA MONTANA ROOT 6 [hp_X] in 1 mL BOS TAURUS FRONTAL LOBE (UNII: R8970AT87X) (BOS TAURUS FRONTAL LOBE - UNII:R8970AT87X) BOS TAURUS FRONTAL LOBE 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 TEMPORAL LOBE (UNII: 490XI1KB4S) (SUS SCROFA TEMPORAL LOBE - UNII:490XI1KB4S) SUS SCROFA TEMPORAL LOBE 8 [hp_X] in 1 mL SILVER SULFIDE (UNII: 9ZB10YHC1C) (SILVER CATION - UNII:57N7B0K90A) SILVER SULFIDE 20 [hp_X] in 1 mL ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE 30 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-1163-1 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(48951-1163)