NDC product
MEB Puri-vega
NDC 81488-013 · Kadesh Incoporation Co,Ltd
Key facts
| Product NDC | 81488-013 |
|---|---|
| Proprietary name | MEB Puri-vega |
| Nonproprietary name | MEB Puri-Vega |
| Substances | CALCIUM FLUORIDE, MAGNESIUM SULFATE HEPTAHYDRATE, SODIUM NITRATE, ZINC, FERROSOFERRIC PHOSPHATE, MAGNESIUM CHLORIDE, SILICON DIOXIDE, SULFUR |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Kadesh Incoporation Co,Ltd |
| 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 | Aug 22, 2023 |
| 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: