NDC product
XTRA Squeeze Antibacterial Hand Juicy Orange
NDC 51628-4442 · MY IMPORTS USA LLC
Key facts
| Product NDC | 51628-4442 |
|---|---|
| Proprietary name | XTRA Squeeze Antibacterial Hand Juicy Orange |
| Nonproprietary name | Benzalkonium Chloride |
| Substances | BENZALKONIUM CHLORIDE |
| Dosage form | GEL |
| Route | TOPICAL |
| Labeler | MY IMPORTS USA LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M003 |
| Marketing start | Mar 14, 2025 |
| 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: