dermveda ULTRA BALANITIS RELIEF NDC 83819-987

NDC codes

FDA NDC Directory

Product NDC (as listed)83819-987Labeler and product segments. Claims need a package NDC.

Product NDC at billing width83819-0987Add 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
83819-987-02	83819098702	60 mL in 1 JAR (83819-987-02)Marketed from Aug 11, 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 BALANITIS RELIEF
Generic name (nonproprietary): cardiospermum, curcuma longa
Active ingredients: Cardiospermum halicacabum flowering top — 10 [hp_X]/60mLTurmeric — 10 [hp_C]/60mL
Dosage form: Solution
Route: Topical
Labeler: Celcius Corp.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 11, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 83819-987_7659bda6-ed60-4559-a80a-96d5d030fd1dSPL ID 7659bda6-ed60-4559-a80a-96d5d030fd1dSPL set ID ab44b4af-f712-411e-9c2a-92fedb931ef2UNII MZP2508BRR, 856YO1Z64F

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

N483819098702 followed by a unit qualifier and the quantity

Package 83819-0987-02. 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 Aug 11, 2026.

Indications (excerpt from the label)

Uses • Ask your Physician before using this for self-treatment. Provides temporary relief from Skin Inflammation, Irritation and/or tingling caused by Genital Balanitis.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)