NDC product
Insomnia HP
NDC 43857-0142 · BioActive Nutritional, Inc.
Key facts
| Product NDC | 43857-0142 |
|---|---|
| Proprietary name | Insomnia |
| Nonproprietary name | Arsenicum Album, Coffea Cruda, Kali Carbonicum, Magnesia Carbonica, Nux Vomica, Passiflora Incarnata, Sepia, Valeriana Officinalis |
| Substances | ARSENIC TRIOXIDE, ARABICA COFFEE BEAN, POTASSIUM CARBONATE, MAGNESIUM CARBONATE, STRYCHNOS NUX-VOMICA SEED, PASSIFLORA INCARNATA FLOWERING TOP, SEPIA OFFICINALIS JUICE, VALERIAN |
| 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], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC] and 3 more |
| Marketing start | Apr 9, 2013 |
| Listing certified through | Dec 31, 2027 |
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: