NDC product
Inflammation
NDC 43742-1303 · Deseret Biologicals, Inc.
Key facts
| Product NDC | 43742-1303 |
|---|---|
| Proprietary name | Inflammation |
| Nonproprietary name | Arnica Montana, Benzoicum Acidum, Echinacea (Angustifolia), Apis Mellifica, Baptisia Tinctoria, Dulcamara, Eucalyptus Globulus, Solanum Nigrum, Eupatorium Perfoliatum, Bryonia (Alba), Colchicum Autumnale, Mercurialis Perennis and 1 more |
| Substances | ARNICA MONTANA WHOLE, BENZOIC ACID, ECHINACEA ANGUSTIFOLIA WHOLE, APIS MELLIFERA, BAPTISIA TINCTORIA ROOT, SOLANUM DULCAMARA TOP, EUCALYPTUS GLOBULUS LEAF, SOLANUM NIGRUM WHOLE, EUPATORIUM PERFOLIATUM FLOWERING TOP, BRYONIA ALBA ROOT, COLCHICUM AUTUMNALE BULB, MERCURIALIS PERENNIS WHOLE and 1 more |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Deseret Biologicals, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Ammonium Ion Binding Activity [MoA], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE] and 2 more |
| Marketing start | Jul 10, 2018 |
| Marketing end | Dec 1, 2028 |
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