NDC product
ThroatSpray
NDC 44911-0450 · Energique, Inc.
Key facts
| Product NDC | 44911-0450 |
|---|---|
| Proprietary name | ThroatSpray |
| Nonproprietary name | Echinacea (Angustifolia), Eugenia Caryophyllata, Glycerinum, Myrrha, Salvia Officinalis, Spilanthes Oleracea, Thymus Serpyllum, Baptisia Tinctoria, Phytolacca Decandra, Hydrastis Canadensis, Apis Mellifica, Belladonna and 3 more |
| Substances | ECHINACEA ANGUSTIFOLIA WHOLE, CLOVE, GLYCERIN, MYRRH, SAGE, ACMELLA OLERACEA FLOWERING TOP, THYMUS SERPYLLUM WHOLE, BAPTISIA TINCTORIA ROOT, PHYTOLACCA AMERICANA ROOT, GOLDENSEAL, APIS MELLIFERA, ATROPA BELLADONNA and 3 more |
| Dosage form | SPRAY |
| Route | ORAL |
| Labeler | Energique, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Glycerol [CS] and 7 more |
| Marketing start | Mar 13, 2018 |
| Marketing end | Oct 3, 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