NDC product
Spineforce S-HP
NDC 43857-0605 · BioActive Nutritional, Inc.
Key facts
| Product NDC | 43857-0605 |
|---|---|
| Proprietary name | Spineforce S-HP |
| Nonproprietary name | Aconitum Napellus, Aesculus Hippocastanum, Colchicum Autumnale, Hypericum Perforatum, Magnesia Phosphorica, Plumbum Metallicum, Rhus Tox, Arnica Montana |
| Substances | ACONITUM NAPELLUS WHOLE, HORSE CHESTNUT, COLCHICUM AUTUMNALE BULB, HYPERICUM PERFORATUM WHOLE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, LEAD, TOXICODENDRON PUBESCENS LEAF, ARNICA MONTANA WHOLE |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | BioActive Nutritional, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA] and 2 more |
| Marketing start | Jun 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: