NDC 43857-0802 – Fng I

Echinacea Angustifolia Whole 3 [hp_X]/mL; Lomatium Dissectum Root 3 [hp_X]/mL; Nasturtium Officinale 3 [hp_X]/mL; Tabebuia Impetiginosa Bark 3 [hp_X]/mL;… · Liquid · Oral

Human Otc Drug

Product NDC43857-0802

Product details

Brand name
Fng I
Generic name
Echinacea (Angustifolia), Lomatium Dissectum, Nasturtium Aquaticum, Tabebuia Impetiginosa, Condurango, Ginkgo Biloba, Ligusticum Porteri, Hydrastis Canadensis, Astragalus Membranaceus, Propolis, Glandula Suprarenalis Bovine, Thymus (Bovine), Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Phytolacca Decandra, Sepia, Alternaria Tenuis Nees, Aspergillus Niger, Candida Albicans, Candida Parapsilosis, Torula Cerevisiae, Mucor Racemosus, Rhizopus Nigricans
Labeler
BioActive Nutritional, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
January 20, 2026
Listing expires
December 31, 2027
Pharmacologic class
Non-Standardized Food Allergenic Extract; Non-Standardized Fungal Allergenic Extract; Non-Standardized Fungal Allergenic Extract; Non-Standardized Fungal Allergenic Extract; Non-Standardized Fungal Allergenic Extract; Non-Standardized Fungal Allergenic Extract; Non-Standardized Fungal Allergenic Extract; Non-Standardized Fungal Allergenic Extract; Non-Standardized Plant Allergenic Extract

Active ingredients

Uses, dosage, side effects and warnings for Fng I →

Package NDC codes (1)

Package NDCDescriptionSince
43857-0802-130 mL in 1 BOTTLE, DROPPER (43857-0802-1)Jan 20, 2026