NDC product
Blistex Medicated Variety Pack (Blistex Medicated Berry Lip Balm, Blistex Medicated Lip Balm, Blistex Medicated Lip)
NDC 10157-9901 · Blistex Inc
Key facts
| Product NDC | 10157-9901 |
|---|---|
| Proprietary name | Blistex Medicated Variety Pack (Blistex Medicated Berry Lip Balm, Blistex Medicated Lip Balm, Blistex Medicated Lip) |
| Labeler | Blistex Inc |
| Marketing category | OTC MONOGRAPH FINAL |
| Application number | part347 |
| Marketing start | Nov 20, 2018 |
| Marketing end | Jan 30, 2020 |
| Listing certified through | Jan 30, 2020 |
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: