NDC product
C02 FIBROZOLVE
NDC 63479-0302 · Apex Energetics Inc.
Key facts
| Product NDC | 63479-0302 |
|---|---|
| Proprietary name | C02 |
| Nonproprietary name | APIS MELLIFICA, AURUM MURIATICUM NATRONATUM, BERBERIS VULGARIS, BOS TAURUS PITUITARUM POSTERIUM, CALCAREA FLUORICA, CALCAREA IODATA, CONIUM MACULATUM, FRAXINUS AMERICANA, HYDRASTIS CANADENSIS, HYDROFLUORICUM ACIDUM, LAPIS ALBUS, PANCREATINUM and 6 more |
| Substances | CALCIUM HEXAFLUOROSILICATE, FRAXINUS AMERICANA BARK, LACTIC ACID, L-, ALLYLTHIOUREA, THUJA OCCIDENTALIS LEAFY TWIG, GOLDENSEAL, HYDROFLUORIC ACID, PANCRELIPASE, SODIUM TETRACHLOROAURATE, THYROID, UNSPECIFIED, CALCIUM FLUORIDE, SEPIA OFFICINALIS JUICE and 6 more |
| Dosage form | SOLUTION/ DROPS |
| Route | SUBLINGUAL |
| Labeler | Apex Energetics Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Bee Venoms [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS] and 7 more |
| Marketing start | Feb 15, 1995 |
| Listing certified through | Dec 31, 2027 |
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: