NDC product
GUNA DIGESTION PLUS
NDC 17089-475 · Guna spa
Key facts
| Product NDC | 17089-475 |
|---|---|
| Proprietary name | GUNA DIGESTION PLUS |
| Nonproprietary name | pork liver - lycopodium clavatum spore - strychnos nux vomica seed - sus scrofa pancreas - aethusa cynapium - |
| Substances | PORK LIVER, LYCOPODIUM CLAVATUM SPORE, SUS SCROFA PANCREAS, AETHUSA CYNAPIUM, STRYCHNOS NUX-VOMICA SEED |
| 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], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] and 1 more |
| 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: