Label: CARDINORMA- arnica montana root, activated charcoal, potassium carbonate, lachesis muta venom, nerium oleander leaf, tobacco leaf, peumus boldus leaf, and crataegus fruit solution/ drops
- NDC Code(s): 59469-109-10
- Packager: PEKANA Naturheilmittel GmbH
- 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.
Updated November 30, 2018
If you are a consumer or patient please visit this version.
- ACTIVE INGREDIENT
Ingredients: Arnica montana 4X Carbo vegetabilis 8X Kalium carbonicum 4X Lachesis muta 8X Nerium oleander 4X Nicotiana tabacum 6X Peumus boldus (Boldo) 4X Crataegus 15.74 mg/ml
Selected ingredients prepared by spagyric processes.Close
- INACTIVE INGREDIENT
Contains 20% alcohol by volume.Close
For support of proper heart function. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.
Unless otherwise prescribed, adults take 15-20 drops, 3 times per day. For pediatric dosages, consult your practitioner.Close
If symptoms persist, contact a licensed practitioner. If you have known sensitivity to any of the ingredients, please consult your licensed practitioner before use. If you are pregnant or nursing a baby, seek the advice of a health care professional before use.
Do not use this product if tamper evident strip is broken or removed from base of cap.
To report adverse events, contact BioResource at 321B Blodgett Street, Cotati, CA 94931Close
- SPL UNCLASSIFIED SECTION
Cotati, CA 94931
- PRINCIPAL DISPLAY PANEL - 50 ml Bottle Box
For support of proper
1.7 FL OZ
- INGREDIENTS AND APPEARANCE
arnica montana root, activated charcoal, potassium carbonate, lachesis muta venom, nerium oleander leaf, tobacco leaf, peumus boldus leaf, and crataegus fruit solution/ drops
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59469-109 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Arnica montana Root (UNII: MUE8Y11327) (Arnica montana Root - UNII:MUE8Y11327) Arnica montana Root 4 [hp_X] in 50 mL Activated Charcoal (UNII: 2P3VWU3H10) (Activated Charcoal - UNII:2P3VWU3H10) Activated Charcoal 8 [hp_X] in 50 mL Potassium carbonate (UNII: BQN1B9B9HA) (Carbonate Ion - UNII:7UJQ5OPE7D) Potassium carbonate 4 [hp_X] in 50 mL Lachesis Muta Venom (UNII: VSW71SS07I) (Lachesis Muta Venom - UNII:VSW71SS07I) Lachesis Muta Venom 8 [hp_X] in 50 mL Nerium oleander Leaf (UNII: 7KV510R6H6) (Nerium Oleander Leaf - UNII:7KV510R6H6) Nerium oleander Leaf 4 [hp_X] in 50 mL Tobacco Leaf (UNII: 6YR2608RSU) (Tobacco Leaf - UNII:6YR2608RSU) Tobacco Leaf 6 [hp_X] in 50 mL Peumus boldus Leaf (UNII: Q4EWM09M3O) (Peumus Boldus Leaf - UNII:Q4EWM09M3O) Peumus boldus Leaf 4 [hp_X] in 50 mL Crataegus Fruit (UNII: Q21UUL2105) (Crataegus Fruit - UNII:Q21UUL2105) Crataegus Fruit 787 mg in 50 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Alcohol (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59469-109-10 1 in 1 BOX 12/11/2008 1 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 12/11/2008 Labeler - PEKANA Naturheilmittel GmbH (320344542) Establishment Name Address ID/FEI Business Operations PEKANA Naturheilmittel GmbH 320344542 MANUFACTURE(59469-109)