Label: EMVITA 5- bufo rana, cuprum metallicum, glandula suprarenalis, phosphorus, pulsatilla, zincum metallicum liquid
- NDC Code(s): 66343-092-60
- Packager: RUBIMED AG
- 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 December 21, 2022
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ACTIVE INGREDIENT
Drug Facts Active Ingredients: (HPUS*) 16.7% of each
Bufo rana 800C Cuprum metallicum 18LM
Glandula suprarenalis 21X Phosphorus 21X
Pulsatilla 16LM Zincum metallicum 21X*The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States. †Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
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INGREDIENTS AND APPEARANCE
EMVITA 5
bufo rana, cuprum metallicum, glandula suprarenalis, phosphorus, pulsatilla, zincum metallicum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66343-092 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BUFO BUFO CUTANEOUS GLAND (UNII: Q59QU6N72Q) (BUFO BUFO CUTANEOUS GLAND - UNII:Q59QU6N72Q) BUFO BUFO CUTANEOUS GLAND 800 [hp_C] in 60 mL COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER 18 [hp_M] in 60 mL SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (SUS SCROFA ADRENAL GLAND - UNII:398IYQ16YV) SUS SCROFA ADRENAL GLAND 21 [hp_X] in 60 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 21 [hp_X] in 60 mL PULSATILLA VULGARIS WHOLE (UNII: I76KB35JEV) (ANEMONE PULSATILLA - UNII:I76KB35JEV) PULSATILLA VULGARIS WHOLE 16 [hp_M] in 60 mL ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS) ZINC 21 [hp_X] in 60 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66343-092-60 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/21/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/21/2022 Labeler - RUBIMED AG (480582035)