Label: EMVITA 10- agnus castus, arum triph, hepar sulph calc, lachesis, pancreas, petroleum liquid
- NDC Code(s): 66343-097-60
- 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
Agnus castus 21X Arum triph 18LM
Hepar Sulph calc 800C Lachesis LM16
Pancreas 21X Petroleum 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 10
agnus castus, arum triph, hepar sulph calc, lachesis, pancreas, petroleum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66343-097 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHASTE TREE FRUIT (UNII: 433OSF3U8A) (CHASTE TREE - UNII:433OSF3U8A) CHASTE TREE FRUIT 21 [hp_X] in 60 mL ARISAEMA TRIPHYLLUM ROOT (UNII: DM64K844DM) (ARISAEMA TRIPHYLLUM ROOT - UNII:DM64K844DM) ARISAEMA TRIPHYLLUM ROOT 18 [hp_M] in 60 mL CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE 800 [hp_C] in 60 mL LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM 16 [hp_M] in 60 mL SUS SCROFA PANCREAS (UNII: 9Y3J3362RY) (SUS SCROFA PANCREAS - UNII:9Y3J3362RY) SUS SCROFA PANCREAS 21 [hp_X] in 60 mL KEROSENE (UNII: 1C89KKC04E) (KEROSENE - UNII:1C89KKC04E) KEROSENE 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:66343-097-60 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)