NDC product
Chavita 4
NDC 66343-085 · RUBIMED AG
Key facts
| Product NDC | 66343-085 |
|---|---|
| Proprietary name | Chavita 4 |
| Nonproprietary name | Aur met, Crataegus, Cetraria, Eucalyptus globulus, Ferrum met, Thymus gland, Zinc val |
| Substances | GOLD, HAWTHORN LEAF WITH FLOWER, CETRARIA ISLANDICA WHOLE, EUCALYPTUS GLOBULUS LEAF, IRON, BOS TAURUS THYMUS, ZINC VALERATE DIHYDRATE |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | RUBIMED AG |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC] |
| Marketing start | Dec 1, 2022 |
| 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: