Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 43857-0576-01 recalled?

B Force · 30 mL in 1 BOTTLE, DROPPER (43857-0576-1)

Yes — this exact package was recalled

1 FDA recall names the code 43857-0576-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
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
Strength
ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/mL; LOMATIUM…
Form
Liquid · Oral
Labeler
BioActive Nutritional, Inc.
Type
Human OTC Drug
Product code
43857-0576

Recalls naming this package

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.