Label: EMVITA 1- potassium carbonate, oyster shell calcium carbonate, crude, lachesis muta venom, naja naja venom, pulsatilla vulgaris, sus scrofa ovary, and bos taurus testicle liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 66343-013-50 - Packager: RUBIMED AG
- 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 July 6, 2015
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INGREDIENTS AND APPEARANCE
EMVITA 1
potassium carbonate, oyster shell calcium carbonate, crude, lachesis muta venom, naja naja venom, pulsatilla vulgaris, sus scrofa ovary, and bos taurus testicle liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66343-013 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE 800 [hp_C] in 1 mL OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 16 [hp_M] in 1 mL LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM 18 [hp_M] in 1 mL NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (NAJA NAJA VENOM - UNII:ZZ4AG7L7VM) NAJA NAJA VENOM 21 [hp_X] in 1 mL PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS 21 [hp_X] in 1 mL SUS SCROFA OVARY (UNII: S7YTV04R8O) (SUS SCROFA OVARY - UNII:S7YTV04R8O) SUS SCROFA OVARY 21 [hp_X] in 1 mL BOS TAURUS TESTICLE (UNII: PR4RXL6G2H) (BOS TAURUS TESTICLE - UNII:PR4RXL6G2H) BOS TAURUS TESTICLE 21 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength Alcohol (UNII: 3K9958V90M) 0.4 mL in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66343-013-50 50 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 05/07/2015 Labeler - RUBIMED AG (480582035) Establishment Name Address ID/FEI Business Operations RUBIMED AG 480582035 MANUFACTURE(66343-013) Establishment Name Address ID/FEI Business Operations Omida AG 483268348 MANUFACTURE(66343-013)