NDC product
MYCCombination
NDC 43742-2108 · Deseret Biologicals, Inc.
Key facts
| Product NDC | 43742-2108 |
|---|---|
| Proprietary name | MYCCombination |
| Nonproprietary name | Allium Cepa, Echinacea (Echinacea Angustifolia), Natrum Sulphuricum, Kali Carbonicum, Sanguinaria Canadensis, Agaricus Muscarius, Antimonium Tartaricum, Arsenicum Iodatum, Carbolicum Acidum, Cinchona Officinalis, Ferrum Metallicum, Phytolacca Decandra and 7 more |
| Substances | ONION, ECHINACEA ANGUSTIFOLIA WHOLE, SODIUM SULFATE, POTASSIUM CARBONATE, SANGUINARIA CANADENSIS ROOT, AMANITA MUSCARIA FRUITING BODY, ANTIMONY POTASSIUM TARTRATE, ARSENIC TRIIODIDE, PHENOL, CINCHONA OFFICINALIS BARK, IRON, PHYTOLACCA AMERICANA ROOT and 7 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], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE] and 5 more |
| Marketing start | Dec 20, 2023 |
| Marketing end | Oct 31, 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