NDC product
Humphreys Maravilla
NDC 0219-0204 · Humphreys Pharmacal, Incorporated
Key facts
| Product NDC | 0219-0204 |
|---|---|
| Proprietary name | Humphreys Maravilla |
| Nonproprietary name | witch hazel |
| Substances | WITCH HAZEL |
| Dosage form | LIQUID |
| Route | TOPICAL |
| Labeler | Humphreys Pharmacal, Incorporated |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M016 |
| Marketing start | Jan 11, 1955 |
| 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: