NDC 43742-1622 – Fng

Berberis Vulgaris Root Bark 3 [hp_X]/mL; Horseradish 3 [hp_X]/mL; Echinacea Angustifolia Whole 3 [hp_X]/mL; Lomatium Dissectum Root 3 [hp_X]/mL; Myrrh 3… · Liquid · Oral

Human Otc Drug

Product NDC43742-1622

Product details

Brand name
Fng
Generic name
Berberis Vulgaris, Cochlearia Armoracia, Echinacea (Angustifolia), Lomatium Dissectum, Myrrha, Hydrastis Canadensis, Propolis, Glandula Suprarenalis Suis, Tabebuia Impetiginosa, Thymus (Suis), Formalinum, Carbolicum Acidum, Ferrum Metallicum, Iridium Metallicum, Lycopodium Clavatum, Phosphoricum Acidum, Pulsatilla (Prastensis), Selenium Metallicum, Zincum Metallicum, Adenosinum Triphosphoricum Dinatrum, Methylcobalamin, Sarcolacticum Acidum, Mucor Racemosus, Alternaria Tenuis Nees, Aspergillus N
Labeler
Deseret Biologicals, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
January 15, 2020
Marketing end
May 28, 2029
Pharmacologic class
Non-Standardized Food Allergenic Extract; 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; Standardized Chemical Allergen

Active ingredients

Uses, dosage, side effects and warnings for Fng →

Package NDC codes (1)

Package NDCDescriptionSince
43742-1622-130 mL in 1 BOTTLE, DROPPER (43742-1622-1)Jan 15, 2020

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