Label: EMVITA 27- anacard occ, calcarea carbonica, cerebrum, helleborus niger, mandragora liquid
- NDC Code(s): 66343-114-60
- 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 23, 2022
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ACTIVE INGREDIENT
Drug Facts Active Ingredients: (HPUS*) 20% of each
Anacard occ 18LM Calcarea carbonica 21X
Cerebrum 21X Helleborus niger 800C
Mandragora 16LM*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 27
anacard occ, calcarea carbonica, cerebrum, helleborus niger, mandragora liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66343-114 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 60 mL OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 21 [hp_X] in 60 mL SUS SCROFA CEREBRUM (UNII: 4GB5DQR532) (SUS SCROFA CEREBRUM - UNII:4GB5DQR532) SUS SCROFA CEREBRUM 21 [hp_X] in 60 mL HELLEBORUS NIGER ROOT (UNII: 608DGJ6815) (HELLEBORUS NIGER ROOT - UNII:608DGJ6815) HELLEBORUS NIGER ROOT 800 [hp_C] in 60 mL MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB) (MANDRAGORA OFFICINARUM ROOT - UNII:I2XCB174VB) MANDRAGORA OFFICINARUM ROOT 16 [hp_M] 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:66343-114-60 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/23/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/23/2022 Labeler - RUBIMED AG (480582035)