NDC product
Immune Booster
NDC 27281-049 · Sunway Biotech LLC
Key facts
| Product NDC | 27281-049 |
|---|---|
| Proprietary name | Immune Booster |
| Nonproprietary name | Apis mellifica, Baptisia tinctoria, Carduus marianus, Echinacea angustifolia, Gallum aparine, Mercurius corrosivus, Mercurius sulphuratus ruber, Nitricum acidum, Sulphur iodatum, Thuja occidentalis. |
| Substances | APIS MELLIFERA, BAPTISIA TINCTORIA ROOT, MILK THISTLE, ECHINACEA ANGUSTIFOLIA, GALIUM APARINE, MERCURIC CHLORIDE, MERCURIC SULFIDE, NITRIC ACID, SULFUR IODIDE, THUJA OCCIDENTALIS LEAFY TWIG |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Sunway Biotech LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC] |
| Marketing start | Nov 13, 2013 |
| 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: