NDC 43857-0442 – Cardioforce I

Arnica Montana Whole 3 [hp_X]/mL; Selenicereus Grandiflorus Stem 3 [hp_X]/mL; Capsicum 3 [hp_X]/mL; Digitalis 6 [hp_X]/mL; Potassium Phosphate, Dibasic 6… · Liquid · Oral

Human Otc Drug

Product NDC43857-0442

Product details

Brand name
Cardioforce I
Generic name
Arnica Montana, Cactus Grandiflorus, Capsicum Annuum, Digitalis Purpurea, Kali Phosphoricum, Laurocerasus, Spigelia Anthelmia, Tabacum, Aconitum Napellus, Agaricus Muscarius, Aurum Muriaticum, Glonoinum, Ignatia Amara, Kalmia Latifolia, Latrodectus Mactans, Valeriana Officinalis
Labeler
BioActive Nutritional, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
May 8, 2017
Marketing end
August 9, 2027
Pharmacologic class
Nitrate Vasodilator; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Non-Standardized Plant Allergenic Extract

Active ingredients

Uses, dosage, side effects and warnings for Cardioforce →

Package NDC codes (1)

Package NDCDescriptionSince
43857-0442-130 mL in 1 BOTTLE, DROPPER (43857-0442-1)May 8, 2017

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