NDC product
SunBurnt PLUS Pain Relief
NDC 24330-240 · Welmedix LLC dba Welmedix Consumer Healthcare
Key facts
| Product NDC | 24330-240 |
|---|---|
| Proprietary name | SunBurnt PLUS Pain Relief |
| Nonproprietary name | Lidocaine Hydrochloride |
| Substances | LIDOCAINE HYDROCHLORIDE |
| Dosage form | GEL |
| Route | TOPICAL |
| Labeler | Welmedix LLC dba Welmedix Consumer Healthcare |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH NOT FINAL |
| Application number | part348 |
| Pharmacologic classes | Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE] |
| Marketing start | Mar 15, 2018 |
| 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: