NDC 43857-0576 – B Force

Echinacea Angustifolia Whole 3 [hp_X]/mL; Lomatium Dissectum Root 3 [hp_X]/mL; Myrrh 3 [hp_X]/mL; Nasturtium Officinale 3 [hp_X]/mL; Handroanthus Impetiginosus… · Liquid · Oral

Human Otc Drug 1 recall

Product NDC43857-0576

Product details

Brand name
B Force
Generic name
Echinacea Angustifolia, Lomatium Dissectum, Myrrha, Nasturtium Aquaticum, Tabebuia Impetiginosa, Hydrastis Canadensis, Propolis, Glandula Suprarenalis Suis, Lymph Node (Suis), Spleen (Suis), Thymus (Suis), Thyroidinum (Suis), Arsenicum Album, Belladonna, Hypericum Perforatum, Phosphorus, Botulinum, Colibacillinum Cum Natrum Muriaticum, Proteus (Vulgaris), Pseudomonas Aeruginosa, Proteus (Morgani), Salmonella Typhi Nosode, Clostridium Perfringens
Labeler
BioActive Nutritional, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
May 4, 2021
Marketing end
July 6, 2028
Pharmacologic class
Acetylcholine Release Inhibitor; Neuromuscular Blocker

Active ingredients

Uses, dosage, side effects and warnings for B-Force →

Package NDC codes (1)

Package NDCDescriptionSince
43857-0576-130 mL in 1 BOTTLE, DROPPER (43857-0576-1)May 4, 2021

Recalls mentioning this NDC

Other B-Force products