NDC product
GUNA OSTEO
NDC 17089-473 · Guna spa
Key facts
| Product NDC | 17089-473 |
|---|---|
| Proprietary name | GUNA OSTEO |
| Nonproprietary name | Arnica montana root - CALCIUM FLUORIDE - CALCIUM PHOSPHATE - equisetum hyemale - fumaric acid - SUS SCROFA UMBILICAL CORD - sus scrofa ovary - sus scrofa placenta - comfrey root - succinic acid… |
| Substances | ARNICA MONTANA ROOT, FUMARIC ACID, SUS SCROFA UMBILICAL CORD, SUS SCROFA OVARY, SUS SCROFA PLACENTA, COMFREY ROOT, SUCCINIC ACID, SILICON DIOXIDE, CALCIUM FLUORIDE, CALCIUM PHOSPHATE, EQUISETUM HYEMALE |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE] |
| Marketing start | Feb 17, 2021 |
| 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: