Shingles Nosode 4028 (shingles nosode) NDC 63083-4028

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-4028Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-4028Add 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
63083-4028-2	63083402802	59 mL in 1 BOTTLE, DROPPER (63083-4028-2)Marketed from Aug 15, 1985

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Shingles Nosode 4028Suffix: 4028
Generic name (nonproprietary): shingles nosode
Active ingredients: Echinacea angustifolia whole — 6 [hp_X]/59mLLysine — 6 [hp_X]/59mLDaphne mezereum bark — 6 [hp_X]/59mLToxicodendron pubescens leaf — 6 [hp_X]/59mLSodium chloride — 6 [hp_X]/59mLCroton tiglium seed — 8 [hp_X]/59mLHuman herpesvirus 1 — 200 [hp_X]/59mLRecombinant varicella zoster virus glycoprotein e antigen — 200 [hp_X]/59mLHuman varicella-zoster immune globulin — 200 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health Formulas
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
Identifiers: Product ID 63083-4028_a45a894a-e945-4f1f-81d1-9490db8da397SPL ID a45a894a-e945-4f1f-81d1-9490db8da397SPL set ID e71d917a-af9f-41e9-a3de-cb588db7e022UNII VB06AV5US8, K3Z4F929H6, X2N6E405GV, 6IO182RP7A, 451W47IQ8X, 0HK2GZK66E, 22G38P19RL, COB9FF6I46, 33T61IWL27

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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N463083402802 followed by a unit qualifier and the quantity

Package 63083-4028-02. 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 Jan 8, 2026.

Indications (excerpt from the label)

INDICATIONS For the temporary relief of fatigue or itchy, painful, or red skin.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)