NDC product
Medi Fect Antiseptic Hand Wash
NDC 12745-177 · Medical Chemical Corporation
Key facts
| Product NDC | 12745-177 |
|---|---|
| Proprietary name | Medi Fect |
| Nonproprietary name | Ethyl Alcohol |
| Substances | ALCOHOL, DIAZOLIDINYL UREA |
| Dosage form | LIQUID |
| Route | TOPICAL |
| Labeler | Medical Chemical Corporation |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M003 |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC] |
| Marketing start | May 14, 2001 |
| 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: