NDC product
GENTLE REJUVENATION ULTRA LIGHT REPAIR SPF 30 SUNSCREEN
NDC 62032-131 · Obagi Medical Products, Inc., a division of Valeant Pharmaceuticals North America LLC.
Key facts
| Product NDC | 62032-131 |
|---|---|
| Proprietary name | GENTLE REJUVENATION ULTRA LIGHT REPAIR SPF 30 |
| Labeler | Obagi Medical Products, Inc., a division of Valeant Pharmaceuticals North America LLC. |
| Marketing category | OTC MONOGRAPH FINAL |
| Application number | part352 |
| Marketing start | Oct 15, 2013 |
| Listing certified through | Dec 31, 2017 |
At a glance
- 1–9 Package NDCs
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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: