Label: EMVITA 25- conium maculatum flowering top, magnesium carbonate, apomorphine hydrochloride, lead, lycopodium clavatum spore, and sus scrofa cerebellum liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 66343-037-50 - 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 July 14, 2015
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- PURPOSE
- Ingredients
- TAMPER-EVIDENT
- Direction
- Warnings
- PRINCIPAL DISPLAY PANEL - 50 ml Bottle Label
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INGREDIENTS AND APPEARANCE
EMVITA 25
conium maculatum flowering top, magnesium carbonate, apomorphine hydrochloride, lead, lycopodium clavatum spore, and sus scrofa cerebellum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66343-037 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Conium Maculatum Flowering Top (UNII: Q28R5GF371) (Conium Maculatum Flowering Top - UNII:Q28R5GF371) Conium Maculatum Flowering Top 800 [hp_C] in 1 mL Magnesium Carbonate (UNII: 0E53J927NA) (Carbonate Ion - UNII:7UJQ5OPE7D, Magnesium Cation - UNII:T6V3LHY838) Magnesium Carbonate 16 [hp_M] in 1 mL Apomorphine Hydrochloride (UNII: F39049Y068) (Apomorphine - UNII:N21FAR7B4S) Apomorphine Hydrochloride 18 [hp_M] in 1 mL Lead (UNII: 2P299V784P) (Lead - UNII:2P299V784P) Lead 21 [hp_X] in 1 mL Lycopodium Clavatum Spore (UNII: C88X29Y479) (Lycopodium Clavatum Spore - UNII:C88X29Y479) Lycopodium Clavatum Spore 21 [hp_X] in 1 mL Sus Scrofa Cerebellum (UNII: 49NGK53TPQ) (Sus Scrofa Cerebellum - UNII:49NGK53TPQ) Sus Scrofa Cerebellum 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:66343-037-50 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(66343-037) Establishment Name Address ID/FEI Business Operations Omida AG 483268348 MANUFACTURE(66343-037)