Label: EMVITA 2- calcarea phosphorica, cuprum metallicum, oophorinum, orchitinum, veratrum album, vipera berus liquid
- NDC Code(s): 66343-090-60
- 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 20, 2022
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ACTIVE INGREDIENT
Drug Facts Active Ingredients: (HPUS*) 16.7% of each
Calcarea phosphorica 800C
Cuprum metallicum 18LM
Oophorinum 21X Orchitinum 21X
Veratrum album 16LM Vipera berus 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 2
calcarea phosphorica, cuprum metallicum, oophorinum, orchitinum, veratrum album, vipera berus liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66343-090 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION 800 [hp_C] in 60 mL COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER 18 [hp_M] in 60 mL SUS SCROFA OVARY (UNII: S7YTV04R8O) (SUS SCROFA OVARY - UNII:S7YTV04R8O) SUS SCROFA OVARY 21 [hp_X] in 60 mL BOS TAURUS TESTICLE (UNII: PR4RXL6G2H) (BOS TAURUS TESTICLE - UNII:PR4RXL6G2H) BOS TAURUS TESTICLE 21 [hp_X] in 60 mL VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (VERATRUM ALBUM ROOT - UNII:QNS6W5US1Z) VERATRUM ALBUM ROOT 16 [hp_M] in 60 mL VIPERA BERUS VENOM (UNII: 0ORO6NCA4M) (VIPERA BERUS VENOM - UNII:0ORO6NCA4M) VIPERA BERUS VENOM 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:66343-090-60 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/20/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/20/2022 Labeler - RUBIMED AG (480582035)
