Perfumox 6028 (perfumox) NDC 63083-6028

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-6028Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-6028Add 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
63083-6028-2	63083602802	59 mL in 1 BOTTLE, DROPPER (63083-6028-2)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): Perfumox 6028Suffix: 6028
Generic name (nonproprietary): perfumox
Active ingredients: Schoenocaulon officinale seed — 6 [hp_X]/59mLStrychnos nux-vomica seed — 8 [hp_X]/59mLCananga odorata leaf oil — 15 [hp_X]/59mLAcetone — 60 [hp_X]/59mLPhosphorus — 12 [hp_X]/59mLAmaryllis belladonna whole — 30 [hp_X]/59mLCinnamic acid — 30 [hp_X]/59mLSulfur iodide — 30 [hp_X]/59mLAcetaldehyde — 30 [hp_X]/59mLColchicum autumnale bulb — 60 [hp_X]/59mLBenzene — 60 [hp_X]/59mLEugenol — 60 [hp_X]/59mLIndole-3-carbinol — 60 [hp_X]/59mLCitrus aurantium flower oil — 60 [hp_X]/59mLLiquid petroleum — 100 [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
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 63083-6028_ca626243-b1c9-4e9f-981b-158d91c59a73SPL ID ca626243-b1c9-4e9f-981b-158d91c59a73SPL set ID d27ac082-12fc-477d-a5c0-bb74f29c0e60UNII 6NAF1689IO, 269XH13919, 6W864D0X3X, 1364PS73AF, 27YLU75U4W, 11B89M58UN, U14A832J8D, L6L8KA2AA0, GO1N1ZPR3B, 993QHL78E6, J64922108F, 3T8H1794QW, C11E72455F, D4BGE91OXH, 6ZAE7X688J
Pharmacologic class: Non-Standardized Plant Allergenic Extract; Standardized Chemical Allergen

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

N463083602802 followed by a unit qualifier and the quantity

Package 63083-6028-02. 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 occasional headache, difficulty breathing, runny or stuffy nose, sneezing, or red, itchy skin due to sensitivity to or exposure to perfumes or fragrances.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)