NDC product
SciatiGon-M
NDC 68703-335 · Silver Star Brands
Key facts
| Product NDC | 68703-335 |
|---|---|
| Proprietary name | SciatiGon-M |
| Nonproprietary name | Aconitum napellus, Berberis vulgaris, Chamomilla, Colocynthis, Magnesia phosphorica, Rhus tox |
| Substances | TOXICODENDRON RADICANS LEAF, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, ACONITUM NAPELLUS, CITRULLUS COLOCYNTHIS FRUIT, BERBERIS VULGARIS FRUIT, MATRICARIA RECUTITA |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Silver Star Brands |
| 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 | Jul 1, 2019 |
| 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: