NDC product
dermveda ULTRA FOLLICULITIS TREATMENT
NDC 83819-606 · Celcius Corp.
Key facts
| Product NDC | 83819-606 |
|---|---|
| Proprietary name | dermveda ULTRA FOLLICULITIS TREATMENT |
| Nonproprietary name | Sulfur, Curcuma Longa |
| Substances | SULFUR, TURMERIC |
| Dosage form | CREAM |
| Route | TOPICAL |
| Labeler | Celcius Corp. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | May 27, 2026 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: