NDC product
Mucus and Sinus Mucus and Sinus Symptom Relief
NDC 17312-433 · TRP Company
Key facts
| Product NDC | 17312-433 |
|---|---|
| Proprietary name | Mucus and Sinus |
| Nonproprietary name | Bryonia alba, Hydrastis canadensis, Kali bichromicum, Natrum Muriaticum, Pulsatilla pratensis, Silicea, Stannum metallicum, Thuja occidentalis, Zincum gluconicum |
| Substances | BRYONIA ALBA ROOT, ZINC GLUCONATE, THUJA OCCIDENTALIS LEAFY TWIG, TIN, SILICON DIOXIDE, PULSATILLA PRATENSIS, SODIUM CHLORIDE, POTASSIUM DICHROMATE, GOLDENSEAL |
| Dosage form | SPRAY |
| Route | ORAL |
| Labeler | TRP Company |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE] |
| 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: