NDC product
Headache
NDC 43857-0805 · BioActive Nutritionals, Inc.
Key facts
| Product NDC | 43857-0805 |
|---|---|
| Proprietary name | Headache |
| Nonproprietary name | Melilotus Officinalis, Spigelia Anthelmia, Allium Cepa, Belladonna, Bryonia (Alba), Cimicifuga Racemosa, Gelsemium Sempervirens, Glonoinum, Lachesis Mutus, Magnesia Phosphorica, Nux Vomica, Sanguinaria Canadensis and 1 more |
| Substances | MELILOTUS OFFICINALIS TOP, SPIGELIA ANTHELMIA WHOLE, ONION, ATROPA BELLADONNA, BRYONIA ALBA ROOT, BLACK COHOSH, NITROGLYCERIN, LACHESIS MUTA VENOM, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, STRYCHNOS NUX-VOMICA SEED, SANGUINARIA CANADENSIS ROOT, SILICON DIOXIDE |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | BioActive Nutritionals, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE] and 15 more |
| Marketing start | Sep 10, 2026 |
| 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: