What is NDC 83819-606?

83819-606 is the product NDC for dermveda ULTRA FOLLICULITIS TREATMENT, Sulfur 10 [hp_X]/60mL; Turmeric 10 [hp_C]/60mL cream, listed with the FDA by Celcius Corp.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

dermveda ULTRA FOLLICULITIS TREATMENT (Sulfur, Curcuma Longa).

Celcius Corp., NDC labeler code 83819. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for dermveda ULTRA FOLLICULITIS TREATMENT?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

dermveda ULTRA FOLLICULITIS TREATMENT NDC 83819-606

NDC codes

FDA NDC Directory

Product NDC (as listed)83819-606Labeler and product segments. Claims need a package NDC.

Product NDC at billing width83819-0606Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
83819-606-02	8381906060283819060602	60 mL in 1 JAR (83819-606-02)Marketed from May 27, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): dermveda ULTRA FOLLICULITIS TREATMENT
Generic name (nonproprietary): sulfur, curcuma longa
Active ingredients: Sulfur — 10 [hp_X]/60mLTurmeric — 10 [hp_C]/60mL
Dosage form: Cream
Route: Topical
Labeler: Celcius Corp.NDC labeler code 83819
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 27, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 83819-606_00956a31-f8e0-4aab-816f-718a19f8a8e8SPL ID 00956a31-f8e0-4aab-816f-718a19f8a8e8SPL set ID f43bc300-50bf-421a-81f8-1da7fc829cd0UNII 70FD1KFU70, 856YO1Z64FUPC 0198168316559

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N483819060602 followed by a unit qualifier and the quantity

Package 83819-0606-02. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective May 29, 2026.

Indications (excerpt from the label)

Uses • Temporarily relieves swelling, itching, rash or skin irritation/inflammation.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 83819-606

What is NDC 83819-606?: 83819-606 is the product NDC for dermveda ULTRA FOLLICULITIS TREATMENT, Sulfur 10 [hp_X]/60mL; Turmeric 10 [hp_C]/60mL cream, listed with the FDA by Celcius Corp.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: dermveda ULTRA FOLLICULITIS TREATMENT (Sulfur, Curcuma Longa).
What is the active ingredient?: Sulfur, Turmeric.
Who is the labeler?: Celcius Corp., NDC labeler code 83819. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for dermveda ULTRA FOLLICULITIS TREATMENT?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

dermveda ULTRA FOLLICULITIS TREATMENT (Sulfur, curcuma longa) NDC 83819-606