Data / Drug companies / Gingi-Pak a Division of the Belport
Gingi-Pak a Division of the Belport: 16 products in the FDA NDC directory, labeler code 10129
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Gingi-Pak a Division of the Belport (labeler code 10129) lists 16 products in the FDA National Drug Code Directory, covering 13 finished drugs by generic name. By type: 16 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on March 20, 2024.
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- Labeler code
- 10129
- Products in commercial distribution
- 16
- Packages
- 27
- Finished drugs by generic name
- 13
- Prescription products
- 0
- Over the counter products
- 16
- Flagged as original packager
- 16 of 16 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- June 26, 1987
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Over the counter monograph drugs | 10 | 62.5% |
| Other unapproved drugs | 6 | 37.5% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 16 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| 1.7% hydrogen peroxide | 3 | 1 |
| Benzocaine | 2 | 110 |
| Gingicaine gel, pina colada flavor | 1 | 1 |
| Ferric sulfate | 1 | 1 |
| Gingicaine gel, cherry flavor | 1 | 1 |
| Aluminum chloride 25% | 1 | 1 |
| Gingicaine gel strawberry flavor | 1 | 1 |
| Gingicaine gel, mint julep flabvor | 1 | 1 |
| Epinephrine hydrochloride | 1 | 1 |
| Gingicaine gel, chocolate mint flavor | 1 | 1 |
| Gingicaine gel, cotton candy flavor | 1 | 1 |
| Gingicaine gel banana flavor | 1 | 1 |
| Gingicaine gel variety pak | 1 | 1 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Gel | 13 | 81.2% |
| Solution | 3 | 18.8% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Standardized Chemical Allergen | 10 |
| Parenteral Iron Replacement | 1 |
| Phosphate Binder | 1 |
| Catecholamine | 1 |
| alpha-Adrenergic Agonist | 1 |
| beta-Adrenergic Agonist | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| UltraCare Anesthetic Gel | 10129-072 | Gel | Over the counter monograph drugs | March 20, 2024 |
| UltraCare Anesthetic Gel | 10129-071 | Gel | Over the counter monograph drugs | February 8, 2023 |
| Perio Armor | 10129-032 | Gel | Other unapproved drugs | October 25, 2022 |
| Perio Armor | 10129-019 | Gel | Other unapproved drugs | August 15, 2022 |
| Perio Armor | 10129-018 | Gel | Other unapproved drugs | August 15, 2022 |
| Gingicaine Gel Variety Pak | 10129-070 | Gel | Over the counter monograph drugs | June 9, 2014 |
| GingiCaine gel, Cherry | 10129-715 | Gel | Over the counter monograph drugs | June 21, 1999 |
| GingiCaine Gel, Mint Julep | 10129-063 | Gel | Over the counter monograph drugs | July 13, 1998 |
| Gingicaine Gel Strawberry | 10129-036 | Gel | Over the counter monograph drugs | July 6, 1993 |
| GingiCaine Gel | 10129-035 | Gel | Over the counter monograph drugs | July 6, 1993 |
| GingiCaine Gel, Chocolate Mint | 10129-034 | Gel | Over the counter monograph drugs | July 6, 1993 |
| GingiCaine Gel, Pina Colada | 10129-033 | Gel | Over the counter monograph drugs | July 6, 1993 |
| GingiCaine Gel, Cotton Candy Flavor | 10129-037 | Gel | Over the counter monograph drugs | March 26, 1993 |
| Gingi-Aid Solution | 10129-017 | Solution | Other unapproved drugs | April 4, 1990 |
| Orostat 8% | 10129-006 | Solution | Other unapproved drugs | April 4, 1990 |
| Stasis | 10129-031 | Solution | Other unapproved drugs | June 26, 1987 |
CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.