NDC product
GUNA-DIGEST
NDC 17089-301 · Guna spa
Key facts
| Product NDC | 17089-301 |
|---|---|
| Proprietary name | GUNA-DIGEST |
| Nonproprietary name | angelica archangelica root - anisum - artemisia abrotanum flowering top - ascorbic acid - citrullus colocynthis fruit pulp - gentiana lutea root - melatonin - niacin - pancrelipase amylase… |
| Substances | ARTEMISIA ABROTANUM FLOWERING TOP, PANCRELIPASE AMYLASE, ANGELICA ARCHANGELICA ROOT, ANISUM, ASCORBIC ACID, CITRULLUS COLOCYNTHIS FRUIT PULP, SUS SCROFA DIENCEPHALON, SUS SCROFA DUODENUM, SUS SCROFA GALLBLADDER, GENTIANA LUTEA ROOT, PORK LIVER, PANCRELIPASE LIPASE and 9 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Ascorbic Acid [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Nicotinic Acid [EPC] and 5 more |
| Marketing start | Dec 21, 2018 |
| 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: