Data / Drug companies / KC Pharmaceuticals, Inc.
KC Pharmaceuticals, Inc.: 14 products in the FDA NDC directory, labeler code 55651
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
KC Pharmaceuticals, Inc. (labeler code 55651) lists 14 products in the FDA National Drug Code Directory, covering 10 finished drugs by generic name. By type: 14 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on March 25, 2026.
The request: Watch KC Pharmaceuticals, Inc. (FDA labeler code 55651): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 55651
- Products in commercial distribution
- 14
- Packages
- 14
- Finished drugs by generic name
- 10
- Prescription products
- 0
- Over the counter products
- 14
- Flagged as original packager
- 14 of 14 products that carry the flag
- Started marketing in the last 12 months
- 5
- Earliest marketing start
- August 28, 2003
- 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 | 14 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 14 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Carboxymethylcellulose sodium | 3 | 30 |
| Glycerin, naphazoline hydrochloride | 2 | 11 |
| Tetrahydrozoline hydrochloride, zinc sulfate | 1 | 1 |
| Carboxymethylcellulose sodium, glycerin | 1 | 6 |
| Polyethylene glycol 400, propylene glycol | 1 | 25 |
| Tetrahydrolizine hcl | 1 | 2 |
| Purified water | 1 | 10 |
| Glycerin, hypromellose, polyethylene glycol 400 | 1 | 13 |
| Tetrahydrozoline hydrochloride | 1 | 3 |
| Polyvinyl alcohol, povidone | 1 | 18 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Solution/ drops | 10 | 71.4% |
| Solution | 4 | 28.6% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Artificial Tears Lubricant Eye Drops | 55651-115 | Solution/ drops | Over the counter monograph drugs | March 25, 2026 |
| Lubricant Eye Drops | 55651-105 | Solution/ drops | Over the counter monograph drugs | March 15, 2026 |
| Lubricant Eye Drops | 55651-510 | Solution/ drops | Over the counter monograph drugs | February 25, 2026 |
| Redness and Dry Eye Relief | 55651-620 | Solution | Over the counter monograph drugs | December 26, 2025 |
| Original Redness Reliever | 55651-063 | Solution/ drops | Over the counter monograph drugs | December 26, 2025 |
| Medics Choice Fresh and Soothe | 55651-200 | Solution/ drops | Over the counter monograph drugs | August 1, 2025 |
| Medics Choice Soothing Eye Wash | 55651-555 | Solution | Over the counter monograph drugs | November 30, 2024 |
| Medics Choice Fresh and Soothe Lubricant Eye Drops | 55651-999 | Solution/ drops | Over the counter monograph drugs | September 1, 2024 |
| Medics Choice Eye Drops Maximum Redness Relief | 55651-059 | Solution | Over the counter monograph drugs | March 27, 2023 |
| Medics Choice Lubricant Eye Drops | 55651-030 | Solution | Over the counter monograph drugs | February 10, 2020 |
| Medics Choice Eye Drops Advanced | 55651-025 | Solution/ drops | Over the counter monograph drugs | December 9, 2003 |
| Artificial Tears | 55651-008 | Solution/ drops | Over the counter monograph drugs | November 25, 2003 |
| Medics Choice Eye Drops Seasonal Relief | 55651-024 | Solution/ drops | Over the counter monograph drugs | October 23, 2003 |
| Medics Choice Eye Drops Original Redness Reliever | 55651-005 | Solution/ drops | Over the counter monograph drugs | August 28, 2003 |
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.