NDC product
NUMSTAT Antiseptic and Pain Relieving Prep Pad
NDC 65282-1815 · Spectra Medical Devices, LLC
Key facts
| Product NDC | 65282-1815 |
|---|---|
| Proprietary name | NUMSTAT Antiseptic and Pain Relieving Prep Pad |
| Nonproprietary name | alcohol, menthol, and benzocaine prep pad |
| Substances | BENZOCAINE, ISOPROPYL ALCOHOL, MENTHOL |
| Dosage form | SWAB |
| Route | TOPICAL |
| Labeler | Spectra Medical Devices, LLC |
| 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 | Jan 1, 2023 |
| 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: