NDC product
Somineze
NDC 43857-0379 · BioActive Nutritional, Inc.
Key facts
| Product NDC | 43857-0379 |
|---|---|
| Proprietary name | Somineze |
| Nonproprietary name | Humulus Lupulus, Passiflora Incarnata, Valeriana Officinalis, Ambrosia Artemisiaefolia, Arsenicum Album, Coffea Tosta, Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Silicea |
| Substances | HOPS, PASSIFLORA INCARNATA FLOWERING TOP, VALERIAN, AMBROSIA ARTEMISIIFOLIA WHOLE, ARSENIC TRIOXIDE, COFFEA ARABICA SEED, ROASTED, LYCOPODIUM CLAVATUM SPORE, STRYCHNOS NUX-VOMICA SEED, PHOSPHORIC ACID, SILICON DIOXIDE |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | BioActive Nutritional, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased IgG Production [PE] and 4 more |
| Marketing start | Oct 14, 2015 |
| 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: