NDC product
Soothe XP
NDC 24208-490 · Bausch & Lomb Incorporated
Key facts
| Product NDC | 24208-490 |
|---|---|
| Proprietary name | Soothe XP |
| Nonproprietary name | light mineral oil and mineral oil |
| Substances | LIGHT MINERAL OIL, MINERAL OIL |
| Dosage form | SOLUTION/ DROPS |
| Route | OPHTHALMIC |
| Labeler | Bausch & Lomb Incorporated |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M018 |
| Marketing start | Aug 26, 2010 |
| Listing certified through | Dec 31, 2027 |
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: