NDC product
GUNA-TONSILS
NDC 17089-235 · Guna spa
Key facts
| Product NDC | 17089-235 |
|---|---|
| Proprietary name | GUNA-TONSILS |
| Nonproprietary name | angelica sinensis root - binetrakin - interleukin-3 - lenograstim - melatonin - reishi - shiitake mushroom - sus scrofa blood - sus scrofa small intestine mucosa lymph follicle - sus scrofa spleen… |
| Substances | ANGELICA SINENSIS ROOT, SUS SCROFA BLOOD, LENOGRASTIM, INTERLEUKIN-11, INTERLEUKIN-3, BINETRAKIN, SHIITAKE MUSHROOM, REISHI, SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE, MELATONIN, SUS SCROFA SPLEEN |
| Dosage form | PELLET |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| 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: