Data / Drug companies / Derma E
Derma E: 14 products in the FDA NDC directory, labeler code 54108
Derma E (labeler code 54108) lists 14 products in the FDA National Drug Code Directory, covering 6 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 July 6, 2026.
SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.
- Labeler code
- 54108
- Products in commercial distribution
- 14
- Packages
- 14
- Finished drugs by generic name
- 6
- 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
- 2
- Products with a marketing end date set
- 1
- Earliest marketing start
- January 1, 2015
- 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 |
|---|---|---|
| Zinc oxide | 6 | 595 |
| Salicylic acid | 4 | 330 |
| Zinc oxide titanium dioxide | 1 | 4 |
| Zinc oxide and titanium dioxide | 1 | 12 |
| Sulfur | 1 | 52 |
| Oatmeal | 1 | 21 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Lotion | 6 | 42.9% |
| Cream | 3 | 21.4% |
| Powder | 2 | 14.3% |
| Gel | 1 | 7.1% |
| Liquid | 1 | 7.1% |
| Cloth | 1 | 7.1% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Sun Protection Mineral SPF 30 | 54108-1487 | Powder | Over the counter monograph drugs | July 6, 2026 |
| Derma E Sun Drops SPF 30 | 54108-1488 | Lotion | Over the counter monograph drugs | June 2, 2026 |
| Derma E Acne Cleansing Pads | 54108-3725 | Cloth | Over the counter monograph drugs | May 23, 2024 |
| Derma E Vitamin C Weightless Moisturizer SPF 45 | 54108-0359 | Lotion | Over the counter monograph drugs | May 22, 2024 |
| Derma E Sun Protection Mineral SPF 30 | 54108-1486 | Powder | Over the counter monograph drugs | February 26, 2024 |
| Derma E Sun Defense SPF 30 | 54108-0418 | Lotion | Over the counter monograph drugs | December 30, 2022 |
| Derma E Sun Defense Face SPF 30 | 54108-0419 | Lotion | Over the counter monograph drugs | December 15, 2022 |
| Derma E Acne Clarifying Mask | 54108-3710 | Cream | Over the counter monograph drugs | December 14, 2022 |
| Derma E Eczema Relief | 54108-8712 | Lotion | Over the counter monograph drugs | June 14, 2022 |
| Derma E Acne Blemish Control Treatment Serum | 54108-3851 | Liquid | Over the counter monograph drugs | February 22, 2022 |
| Derma E Acne Matte Moisturizer | 54108-3900 | Lotion | Over the counter monograph drugs | May 21, 2021 |
| Scar Gel SPF 35 | 54108-8111 | Cream | Over the counter monograph drugs | July 15, 2020 |
| Sun Defense Mineral Sunscreen SPF 30 Face | 54108-0420 | Cream | Over the counter monograph drugs | January 1, 2016 |
| Acne Deep Pore Cleansing Wash | 54108-3700 | Gel | Over the counter monograph drugs | January 1, 2015 |
Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). 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.