NDC product
2.5 Acne Med
NDC 70707-152 · Face Reality, Inc.
Key facts
| Product NDC | 70707-152 |
|---|---|
| Proprietary name | 2.5 Acne Med |
| Nonproprietary name | BENZOYL PEROXIDE |
| Substances | BENZOYL PEROXIDE |
| Dosage form | GEL |
| Route | TOPICAL |
| Labeler | Face Reality, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M006 |
| Marketing start | Nov 23, 2011 |
| Marketing end | Jul 1, 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