NDC product
Bio Glyoxal Phase
NDC 43742-1257 · Deseret Biologicals, Inc.
Key facts
| Product NDC | 43742-1257 |
|---|---|
| Proprietary name | Bio Glyoxal Phase |
| Nonproprietary name | Arnica Montana, Baptisia Tinctoria, Echinacea (Angustifolia), Sanguinaria Canadensis, Eupatorium Perfoliatum, Euphorbium Officinarum, Dopamine Hydrochloride, Phytolacca Decandra, Aconitum Napellus, Argentum Nitricum, Arsenicum Album, Bryonia (Alba) and 13 more |
| Substances | ARNICA MONTANA WHOLE, BAPTISIA TINCTORIA ROOT, ECHINACEA ANGUSTIFOLIA WHOLE, SANGUINARIA CANADENSIS ROOT, EUPATORIUM PERFOLIATUM FLOWERING TOP, EUPHORBIA RESINIFERA RESIN, DOPAMINE HYDROCHLORIDE, PHYTOLACCA AMERICANA ROOT, ACONITUM NAPELLUS WHOLE, SILVER NITRATE, ARSENIC TRIOXIDE, BRYONIA ALBA ROOT and 13 more |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Deseret Biologicals, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] and 2 more |
| Marketing start | Jun 7, 2019 |
| Listing certified through | Dec 31, 2026 |
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 · Source date: