Label: LYCOPUS- lycopus virginicus, spongia tosta, lophophytum leandrii, chininum arsenicosum, calcarea phosphorica, magnesia phosphorica liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 60986-1026-3 - Packager: Marco Pharma International LLC.
- 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 7, 2015
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Active Ingredients
LYCOPUS VIRGINICUS 1XHPUS
SPONGIA TOSTA 1XHPUS
LOPHOPHYTUM LEANDRII 6XHPUS
CHININUM ARSENICOSUM 6XHPUS
CALCAREA PHOSPHORICA 8XHPUS
MAGNESIA PHOSPHORICA 8XHPUS
The letters HPUS indicates that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of United Sates.
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INGREDIENTS AND APPEARANCE
LYCOPUS
lycopus virginicus, spongia tosta, lophophytum leandrii, chininum arsenicosum, calcarea phosphorica, magnesia phosphorica liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60986-1026 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LYCOPUS VIRGINICUS (UNII: TWH5125Q6F) (LYCOPUS VIRGINICUS - UNII:TWH5125Q6F) LYCOPUS VIRGINICUS 1 [hp_X] in 100 mL SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (SPONGIA OFFICINALIS SKELETON, ROASTED - UNII:1PIP394IID) SPONGIA OFFICINALIS SKELETON, ROASTED 1 [hp_X] in 100 mL LOPHOPHYTUM LEANDRII (UNII: 59150S2EOG) (LOPHOPHYTUM LEANDRII - UNII:59150S2EOG) LOPHOPHYTUM LEANDRII 6 [hp_X] in 100 mL QUININE ARSENITE (UNII: 42QO5P0NLM) (QUININE - UNII:A7V27PHC7A) QUININE ARSENITE 6 [hp_X] in 100 mL TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) (PHOSPHATE ION - UNII:NK08V8K8HR) TRIBASIC CALCIUM PHOSPHATE 8 [hp_X] in 100 mL MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 8 [hp_X] in 100 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:60986-1026-3 50 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/01/1992 Labeler - Marco Pharma International LLC. (161994277) Establishment Name Address ID/FEI Business Operations Nestmann Pharma GmbH 323426262 manufacture(60986-1026)