NDC product
GUNA-BOWEL
NDC 17089-293 · Guna spa
Key facts
| Product NDC | 17089-293 |
|---|---|
| Proprietary name | GUNA-BOWEL |
| Nonproprietary name | ALOE - ALUMINUM OXIDE - BRYONIA ALBA ROOT - CHELIDONIUM MAJUS - CHOLECALCIFEROL - COLLINSONIA - FRANGULA ALNUS BARK - NIACIN - PANTOTHENIC ACID - POTASSIUM CARBONATE - RHUBARB - SILYBUM MARIANUM SEED… |
| Substances | ALOE, ALUMINUM OXIDE, BRYONIA ALBA ROOT, SILYBUM MARIANUM SEED, CHELIDONIUM MAJUS, CHOLECALCIFEROL, COLLINSONIA, SUS SCROFA COLON, POTASSIUM CARBONATE, SODIUM CARBONATE, NIACIN, STRYCHNOS NUX-VOMICA SEED and 7 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Nicotinic Acid [EPC] and 7 more |
| Marketing start | May 23, 2006 |
| 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: