NDC product
SunBurnt Advanced After-Sun
NDC 0295-1107 · Denison Pharmaceuticals, LLC.
Key facts
| Product NDC | 0295-1107 |
|---|---|
| Proprietary name | SunBurnt Advanced After-Sun |
| Labeler | Denison Pharmaceuticals, LLC. |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | Jan 1, 2007 |
| Marketing end | Jan 20, 2022 |
| Listing certified through | Jan 20, 2022 |
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: