NDC product
GUNA BOWEL PLUS
NDC 17089-470 · Guna spa
Key facts
| Product NDC | 17089-470 |
|---|---|
| Proprietary name | GUNA BOWEL PLUS |
| Nonproprietary name | ACTIVATED CHARCOAL - ALOE - ALUMINUM OXIDE - BRYONIA ALBA ROOT - CHELIDONIUM MAJUS - COLLINSONIA - FRANGULA ALNUS BARK - LYCOPODIUM CLAVATUM SPORE - POTASSIUM CARBONATE- RHUBARB - STRYCHNOS NUX VOMICA… |
| Substances | ALOE, ALUMINUM OXIDE, BRYONIA ALBA ROOT, SILYBUM MARIANUM SEED, CHELIDONIUM MAJUS, ACTIVATED CHARCOAL, COLLINSONIA, SUS SCROFA PANCREAS, POTASSIUM CARBONATE, SODIUM CARBONATE, LYCOPODIUM CLAVATUM SPORE, STRYCHNOS NUX-VOMICA SEED and 5 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], Non-Standardized Food Allergenic Extract [EPC] and 3 more |
| Marketing start | Jan 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: