NDC product
Sinusforce
NDC 43857-0616 · BioActive Nutritional, Inc.
Key facts
| Product NDC | 43857-0616 |
|---|---|
| Proprietary name | Sinusforce |
| Nonproprietary name | Echinacea (Angustifolia), Nux Moschata, Trigonella Foenum Graecum, Hydrastis Canadensis, Arsenicum Album, Kali Bichromicum, Mercurius Sulphuratus Ruber, Pulsatilla (Vulgaris), Sepia, Mercurius Solubilis |
| Substances | ECHINACEA ANGUSTIFOLIA WHOLE, NUTMEG, FENUGREEK SEED, GOLDENSEAL, ARSENIC TRIOXIDE, POTASSIUM DICHROMATE, MERCURIC SULFIDE, PULSATILLA VULGARIS WHOLE, SEPIA OFFICINALIS JUICE, MERCURIUS SOLUBILIS |
| 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], Non-Standardized Food Allergenic Extract [EPC] and 3 more |
| Marketing start | Sep 15, 2021 |
| 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: