NDC product
Whole System EEP
NDC 61657-0208 · White Manufacturing Inc. DBA Micro-West
Key facts
| Product NDC | 61657-0208 |
|---|---|
| Proprietary name | Whole System EEP |
| Nonproprietary name | MERCURIUS CORROSIVUS, NUX VOMICA, HYOSCYAMINUM, CARCINOSINUM, GRAPHITES, ZINCUM METALLICUM, LILIUM TIGRINUM, CINCHONA OFFICINALIS, CAUSTICUM, COFFEA CRUDA, BELLADONNA, IGNATIA AMARA and 12 more |
| Substances | MERCURIC CHLORIDE, BERBERIS VULGARIS ROOT BARK, LYCOPODIUM CLAVATUM SPORE, SUS SCROFA PANCREAS, BOS TAURUS PITUITARY GLAND, CHELIDONIUM MAJUS, MARSDENIA CONDURANGO BARK, GOLDENSEAL, SENNA LEAF, CEANOTHUS AMERICANUS LEAF, SPONGIA OFFICINALIS SKELETON, ROASTED, SCROPHULARIA NODOSA and 11 more |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | White Manufacturing Inc. DBA Micro-West |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC] and 3 more |
| Marketing start | May 21, 2005 |
| 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: