Label: EMVITA 7- anacard occ, lachesis mutus, phosphorus, glandula sup, lycopodium liquid
- NDC Code(s): 66343-056-50
- Packager: RUBIMED AG
- Category: HUMAN PRESCRIPTION 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 January 21, 2021
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ACTIVE INGREDIENT
Drug Facts
Active Ingredients: (HPUS*) 20% of each
Anacard occ 18LM Glandula sup 21X
Lachesis mutus 800C Lycopodium 16LM
Phosphorus 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.
- INDICATIONS & USAGE
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- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
EMVITA 7
anacard occ, lachesis mutus, phosphorus, glandula sup, lycopodium liquidProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:66343-056 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANACARDIUM OCCIDENTALE FRUIT (UNII: 4A10JR4E7E) (ANACARDIUM OCCIDENTALE FRUIT - UNII:4A10JR4E7E) ANACARDIUM OCCIDENTALE FRUIT 18 [hp_M] in 50 mL LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM 800 [hp_C] in 50 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 21 [hp_X] in 50 mL SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (SUS SCROFA ADRENAL GLAND - UNII:398IYQ16YV) SUS SCROFA ADRENAL GLAND 21 [hp_X] in 50 mL LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE 16 [hp_M] in 50 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:66343-056-50 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/03/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/03/2019 Labeler - RUBIMED AG (480582035)
