Data / Drug companies / Coloplast Corp
Coloplast Corp: 17 products in the FDA NDC directory, labeler code 11701
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Coloplast Corp (labeler code 11701) lists 17 products in the FDA National Drug Code Directory, covering 8 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 July 1, 2021.
The request: Watch Coloplast Corp (FDA labeler code 11701): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 11701
- Products in commercial distribution
- 17
- Packages
- 37
- Finished drugs by generic name
- 8
- Prescription products
- 0
- Over the counter products
- 17
- Flagged as original packager
- 17 of 17 products that carry the flag
- Started marketing in the last 12 months
- 0
- Products with a marketing end date set
- 2
- Earliest marketing start
- June 15, 2009
- 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 | 16 | 94.1% |
| New drug applications (NDA) | 1 | 5.9% |
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 |
|---|---|---|
| Miconazole nitrate | 3 | 101 |
| Petrolatum | 3 | 74 |
| Dimethicone | 3 | 69 |
| Alcohol | 2 | 293 |
| Benzethonium chloride | 2 | 27 |
| Zinc oxide and dimethicone | 2 | 1 |
| Chlorhexidine gluconate 4% | 1 | 11 |
| Zinc oxide | 1 | 595 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Ointment | 4 | 23.5% |
| Cream | 4 | 23.5% |
| Gel | 2 | 11.8% |
| Shampoo | 2 | 11.8% |
| Lotion | 2 | 11.8% |
| Powder | 1 | 5.9% |
| Solution | 1 | 5.9% |
| Paste | 1 | 5.9% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Azole Antifungal | 3 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Antiseptic Solution | 11701-172 | Solution | New drug applications (NDA) | July 1, 2021 |
| Baza Protect | 11701-082 | Cream | Over the counter monograph drugs | April 6, 2020 |
| Critic-Aid Clear | 11701-083 | Ointment | Over the counter monograph drugs | January 22, 2019 |
| Critic Aid Clear AF | 11701-067 | Ointment | Over the counter monograph drugs | June 15, 2009 |
| Critic Aid Clear | 11701-066 | Ointment | Over the counter monograph drugs | June 15, 2009 |
| Sween 24 | 11701-063 | Cream | Over the counter monograph drugs | June 15, 2009 |
| Baza Cleanse and Protect Odor Control | 11701-062 | Lotion | Over the counter monograph drugs | June 15, 2009 |
| Bedside-Care | 11701-053 | Shampoo | Over the counter monograph drugs | June 15, 2009 |
| Bedside-Care Foam (Alcohol Free) | 11701-052 | Shampoo | Over the counter monograph drugs | June 15, 2009 |
| Critic Aid Skin | 11701-050 | Paste | Over the counter monograph drugs | June 15, 2009 |
| Baza Clear | 11701-048 | Ointment | Over the counter monograph drugs | June 15, 2009 |
| Baza Cleanse and Protect | 11701-047 | Lotion | Over the counter monograph drugs | June 15, 2009 |
| Baza Protect | 11701-046 | Cream | Over the counter monograph drugs | June 15, 2009 |
| Baza Antifungal | 11701-045 | Cream | Over the counter monograph drugs | June 15, 2009 |
| Micro-Guard (AF) | 11701-038 | Powder | Over the counter monograph drugs | June 15, 2009 |
| Isagel | 11701-025 | Gel | Over the counter monograph drugs | June 15, 2009 |
| Isagel | 11701-025 | Gel | Over the counter monograph drugs | June 15, 2009 |
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.