NDC product
Natural Relief Cold and Flu Plus Zinc
NDC 17312-431 · TRP Company
Key facts
| Product NDC | 17312-431 |
|---|---|
| Proprietary name | Natural Relief Cold and Flu |
| Nonproprietary name | Allium cepa, Arsenicum album, Bryonia alba, Eupatorium perfoliatum, Gelsemium sempervirens, Natrum muriaticum, Nux vomica, Silicea, Sulphur, Zincum gluconicum |
| Substances | ALLIUM CEPA WHOLE, SILICON DIOXIDE, STRYCHNOS NUX-VOMICA SEED, SODIUM CHLORIDE, BRYONIA ALBA ROOT, GELSEMIUM SEMPERVIRENS WHOLE, EUPATORIUM PERFOLIATUM FLOWERING TOP, ARSENIC TRIOXIDE, SULFUR, ZINC GLUCONATE |
| Dosage form | SPRAY |
| Route | ORAL |
| Labeler | TRP Company |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Increased Histamine Release [PE], Increased IgG Production [PE] and 7 more |
| Marketing start | Aug 6, 2024 |
| 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: