Data / Drug companies / Gentell LLC
Gentell LLC: 17 products in the FDA NDC directory, labeler code 61554
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Gentell LLC (labeler code 61554) lists 17 products in the FDA National Drug Code Directory, covering 15 finished drugs by generic name. By type: 17 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on October 9, 2026.
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- Labeler code
- 61554
- Products in commercial distribution
- 17
- Packages
- 25
- Finished drugs by generic name
- 15
- Prescription products
- 0
- Over the counter products
- 17
- Flagged as original packager
- 16 of 16 products that carry the flag
- Started marketing in the last 12 months
- 17
- Earliest marketing start
- August 1, 2026
- 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 | 17 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 17 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Lanolin | 2 | 7 |
| Dimethicone | 2 | 69 |
| Menthol, zinc oxide | 1 | 5 |
| Zinc oxide | 1 | 595 |
| Bacitracin zinc, neomycin sulfate, polymyxin b | 1 | 1 |
| Aluminum sesquichlorohydrate 15% | 1 | 1 |
| Miconazole nitrate | 1 | 101 |
| Zinc oxide, dimethicone | 1 | 3 |
| Bacitracin zinc | 1 | 39 |
| Aluminum hydroxide gel | 1 | 1 |
| Benzalkonium chloride | 1 | 271 |
| Petrolatum | 1 | 74 |
| Camphor | 1 | 23 |
| Hydrocortisone acetate | 1 | 35 |
| Miconazole nitrate 2% | 1 | 10 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Cream | 8 | 47.1% |
| Ointment | 6 | 35.3% |
| Aerosol, spray | 1 | 5.9% |
| Lotion | 1 | 5.9% |
| Powder | 1 | 5.9% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Azole Antifungal | 2 |
| Aminoglycoside Antibacterial | 1 |
| Polymyxin-class Antibacterial | 1 |
| Corticosteroid | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Claravie | 61554-316 | Powder | Over the counter monograph drugs | October 9, 2026 |
| Claravie | 61554-318 | Ointment | Over the counter monograph drugs | September 9, 2026 |
| Claravie | 61554-317 | Aerosol, spray | Over the counter monograph drugs | September 9, 2026 |
| Claravie | 61554-313 | Ointment | Over the counter monograph drugs | August 24, 2026 |
| Claravie | 61554-310 | Ointment | Over the counter monograph drugs | August 24, 2026 |
| Claravie | 61554-315 | Lotion | Over the counter monograph drugs | August 21, 2026 |
| Claravie | 61554-312 | Cream | Over the counter monograph drugs | August 21, 2026 |
| Claravie | 61554-311 | Cream | Over the counter monograph drugs | August 21, 2026 |
| Claravie | 61554-309 | Ointment | Over the counter monograph drugs | August 20, 2026 |
| Claravie | 61554-308 | Cream | Over the counter monograph drugs | August 20, 2026 |
| Claravie | 61554-305 | Cream | Over the counter monograph drugs | August 20, 2026 |
| ClaraVie | 61554-307 | Cream | Over the counter monograph drugs | August 19, 2026 |
| ClaraVie | 61554-306 | Ointment | Over the counter monograph drugs | August 19, 2026 |
| Claravie Skin Repair Cream | 61554-303 | Cream | Over the counter monograph drugs | August 19, 2026 |
| ClaraVie | 61554-304 | Ointment | Over the counter monograph drugs | August 1, 2026 |
| ClaraVie | 61554-302 | Cream | Over the counter monograph drugs | August 1, 2026 |
| Claravie | 61554-301 | Cream | Over the counter monograph drugs | August 1, 2026 |
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.