Data / Drug companies / Combe Incorporated
Combe Incorporated: 8 products in the FDA NDC directory, labeler code 11509
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Combe Incorporated (labeler code 11509) lists 8 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 8 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on October 8, 2020.
The request: Watch Combe Incorporated (FDA labeler code 11509): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 11509
- Products in commercial distribution
- 8
- Packages
- 8
- Finished drugs by generic name
- 5
- Prescription products
- 0
- Over the counter products
- 8
- Flagged as original packager
- 8 of 8 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- March 1, 1995
- 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 | 5 | 62.5% |
| Generic drugs (ANDA) | 3 | 37.5% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 8 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Miconazole nitrate | 2 | 101 |
| Pramoxine hydrochloride | 2 | 15 |
| Benzocaine and resorcinol | 2 | 2 |
| Tioconazole | 1 | 16 |
| Hydrocortisone acetate | 1 | 35 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Cream | 4 | 50% |
| Cloth | 2 | 25% |
| Kit | 1 | 12.5% |
| Ointment | 1 | 12.5% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Azole Antifungal | 2 |
| Standardized Chemical Allergen | 2 |
| Corticosteroid | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Vagisil brand vagistat | 11509-0825 | Cream | Generic drugs (ANDA) | October 8, 2020 |
| Vagistat | 11509-0426 | Ointment | Generic drugs (ANDA) | July 29, 2020 |
| Vagistat 3 | 11509-0081 | Kit | Generic drugs (ANDA) | March 27, 2018 |
| Vagisil Anti-Itch Creme Maximum Strength Sensitive Skin Formula | 11509-5101 | Cream | Over the counter monograph drugs | January 30, 2016 |
| VAGISIL Anti-Itch Creme Regular Strength | 11509-5103 | Cream | Over the counter monograph drugs | January 1, 2016 |
| VAGISIL Anti-Itch Medicated Wipes Maximum Strength | 11509-5058 | Cloth | Over the counter monograph drugs | June 28, 2005 |
| VAGISIL Anti-Itch Medicated Wipes Maximum Strength | 11509-5035 | Cloth | Over the counter monograph drugs | June 28, 2005 |
| VAGISIL Anti-Itch Medicated Creme Maximum Strength | 11509-4402 | Cream | Over the counter monograph drugs | March 1, 1995 |
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.