Label: HELLEBORUS COMP. B liquid
- NDC Code(s): 48951-5115-1
- Packager: Uriel Pharmacy Inc.
- Category: HUMAN OTC DRUG LABEL
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 December 17, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- WARNINGS
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
HELLEBORUS COMP. B
helleborus comp. b liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-5115 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COLCHICUM AUTUMNALE WHOLE (UNII: W79255C628) (COLCHICUM AUTUMNALE WHOLE - UNII:W79255C628) COLCHICUM AUTUMNALE WHOLE 4 [hp_X] in 1 mL FORMICA RUFA (UNII: 55H0W83JO5) (FORMICA RUFA - UNII:55H0W83JO5) FORMICA RUFA 20 [hp_X] in 1 mL BOS TAURUS SPLEEN (UNII: 190Q9MB3U3) (BOS TAURUS SPLEEN - UNII:190Q9MB3U3) BOS TAURUS SPLEEN 8 [hp_X] in 1 mL ANTIMONY (UNII: 9IT35J3UV3) (ANTIMONY - UNII:9IT35J3UV3) ANTIMONY 17 [hp_X] in 1 mL SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER 12 [hp_X] in 1 mL HELLEBORUS FOETIDUS ROOT (UNII: 332Y7EES96) (HELLEBORUS FOETIDUS ROOT - UNII:332Y7EES96) HELLEBORUS FOETIDUS ROOT 4 [hp_X] in 1 mL EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (EQUISETUM ARVENSE TOP - UNII:1DP6Y6B65Z) EQUISETUM ARVENSE TOP 20 [hp_X] in 1 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 30 [hp_X] in 1 mL LEAD (UNII: 2P299V784P) (LEAD - UNII:2P299V784P) LEAD 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:48951-5115-1 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(48951-5115)