NDC product
GUNA-REACT
NDC 17089-237 · Guna spa
Key facts
| Product NDC | 17089-237 |
|---|---|
| Proprietary name | GUNA-REACT |
| Nonproprietary name | angelica sinensis root - arnica montana - asian ginseng - echinacea angustifolia - fomitopsis pinicola fruiting body - interferon gamma-1b - paeonia officinalis root - pork liver - reishi - silybum… |
| Substances | TURMERIC, ANGELICA SINENSIS ROOT, ARNICA MONTANA, SILYBUM MARIANUM SEED, ECHINACEA ANGUSTIFOLIA, ASIAN GINSENG, PORK LIVER, INTERFERON GAMMA-1B, REISHI, SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE, PAEONIA OFFICINALIS ROOT, FOMITOPSIS PINICOLA FRUITING BODY |
| Dosage form | PELLET |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Interferon gamma [EPC], Interferon-gamma [CS] |
| 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: