NDC product
PreviDent Alcohol Free
NDC 0126-0033 · Colgate Oral Pharmaceuticals, Inc.
Key facts
| Product NDC | 0126-0033 |
|---|---|
| Proprietary name | PreviDent Alcohol Free |
| Nonproprietary name | Sodium Fluoride |
| Substances | SODIUM FLUORIDE |
| Dosage form | MOUTHWASH |
| Route | DENTAL |
| Labeler | Colgate Oral Pharmaceuticals, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing start | Jun 13, 2016 |
| 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: