NDC product
FNG
NDC 43742-1622 · Deseret Biologicals, Inc.
Key facts
| Product NDC | 43742-1622 |
|---|---|
| Proprietary name | FNG |
| Nonproprietary name | Berberis Vulgaris, Cochlearia Armoracia, Echinacea (Angustifolia), Lomatium Dissectum, Myrrha, Hydrastis Canadensis, Propolis, Glandula Suprarenalis Suis, Tabebuia Impetiginosa, Thymus (Suis), Formalinum, Carbolicum Acidum and 13 more |
| Substances | BERBERIS VULGARIS ROOT BARK, HORSERADISH, ECHINACEA ANGUSTIFOLIA WHOLE, LOMATIUM DISSECTUM ROOT, MYRRH, GOLDENSEAL, PROPOLIS WAX, SUS SCROFA ADRENAL GLAND, TABEBUIA IMPETIGINOSA BARK, SUS SCROFA THYMUS, FORMALDEHYDE, PHENOL and 19 more |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Deseret Biologicals, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Fungal Proteins [CS], Increased Histamine Release [PE] and 6 more |
| Marketing start | Jan 15, 2020 |
| Marketing end | May 28, 2029 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory