NDC product
Bite and Itch
NDC 11383-192 · Weeks & Leo Co., Inc.
Key facts
| Product NDC | 11383-192 |
|---|---|
| Proprietary name | Bite and Itch |
| Nonproprietary name | Diphenhydramine Hydrochloride, Pramoxine Hydrochloride |
| Substances | PRAMOXINE HYDROCHLORIDE, DIPHENHYDRAMINE HYDROCHLORIDE |
| Dosage form | LOTION |
| Route | CUTANEOUS |
| Labeler | Weeks & Leo Co., Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M017 |
| Pharmacologic classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
| Marketing start | Jun 15, 2015 |
| 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: