NDC product
Gout Relief 3310-S
NDC 85631-001 · Bispit Canada Ltd.
Key facts
| Product NDC | 85631-001 |
|---|---|
| Proprietary name | Gout Relief 3310-S |
| Nonproprietary name | CELERY SEED MEDICAGO SATIVA WHOLE |
| Substances | LYSIMACHIA CHRISTINAE WHOLE, MEDICAGO SATIVA WHOLE, PUERARIN, SODIUM CHLORIDE, CHICORY ROOT, GLUCOSAMINE HYDROCHLORIDE, BUCKWHEAT, LICORICE, CELERY SEED, MORUS ALBA LEAF |
| Dosage form | CAPSULE |
| Route | ORAL |
| Labeler | Bispit Canada Ltd. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Grain Proteins [EXT], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE] and 4 more |
| Marketing start | May 6, 2025 |
| 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: