NDC 43857-0652 – 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; Dibasic Potassium Phosphate 6… · Liquid · Oral

Human Otc Drug

Product NDC43857-0652

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
January 2, 2025
Listing expires
December 31, 2026
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
43857-0652-130 mL in 1 BOTTLE, DROPPER (43857-0652-1)Jan 2, 2025

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