NDC product
Gingicaine Gel Variety Pak
NDC 10129-070 · Gingi-Pak a Division of the Belport
Key facts
| Product NDC | 10129-070 |
|---|---|
| Proprietary name | Gingicaine Gel Variety Pak |
| Nonproprietary name | Gingicaine Gel Variety Pak |
| Substances | BENZOCAINE |
| Dosage form | GEL |
| Route | DENTAL, ORAL, PERIODONTAL |
| Labeler | Gingi-Pak a Division of the Belport |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M022 |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC] |
| Marketing start | Jun 9, 2014 |
| Listing certified through | Dec 31, 2027 |
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: