What is NDC 63083-6015?

63083-6015 is the product NDC for Opsin II 6015 (opsin ii), Onion 3 [hp_X]/59mL + 11 more ingredients liquid, listed with the FDA by Professional Complementary Health Formulas. It has 1 package NDC, shown above in 10- and 11-digit form.

What is the active ingredient?

Onion, Ambrosia artemisiifolia whole, Euphrasia stricta, Wyethia helenioides root, Naphthalene, Epinephrine, Arundo pliniana root, Schoenocaulon officinale seed, Arsenic trioxide, Histamine dihydrochloride, Sodium chloride, Tobacco leaf.

Professional Complementary Health Formulas, NDC labeler code 63083. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Opsin II 6015?

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.

Opsin II 6015 NDC 63083-6015 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-6015Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-6015Add 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
63083-6015-2	6308360150263083601502	59 mL in 1 BOTTLE, DROPPER (63083-6015-2)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): Opsin II 6015Suffix: 6015
Generic name (nonproprietary): opsin ii
Active ingredients: Onion — 3 [hp_X]/59mLAmbrosia artemisiifolia whole — 3 [hp_X]/59mLEuphrasia stricta — 3 [hp_X]/59mLWyethia helenioides root — 3 [hp_X]/59mLNaphthalene — 4 [hp_X]/59mLEpinephrine — 6 [hp_X]/59mLArundo pliniana root — 6 [hp_X]/59mLSchoenocaulon officinale seed — 6 [hp_X]/59mLArsenic trioxide — 12 [hp_X]/59mLHistamine dihydrochloride — 12 [hp_X]/59mLSodium chloride — 12 [hp_X]/59mLTobacco leaf — 12 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health FormulasNDC labeler code 63083
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Allergens (Chemical structure)Allergens (Chemical structure)Catecholamines (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 63083-6015_7721ddb5-2ec3-4146-9d28-b178fbfc3184SPL ID 7721ddb5-2ec3-4146-9d28-b178fbfc3184SPL set ID 848d620e-ddd5-4787-a4bd-844be7615432UNII 492225Q21H, 9W34L2CQ9A, C9642I91WL, J10PD1AQ0N, 2166IN72UN, YKH834O4BH, ZXE7LB03WC, 6NAF1689IO, S7V92P67HO, 3POA0Q644U, 451W47IQ8X, 6YR2608RSU
Pharmacologic class: Catecholamine; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; alpha-Adrenergic Agonist; beta-Adrenergic Agonist

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

N463083601502 followed by a unit qualifier and the quantity

Package 63083-6015-02. 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 runny nose, sneezing, itching of the nose or throat, and itchy or watery eyes due to sensitivity to inhalant allergens.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-6015

What is NDC 63083-6015?: 63083-6015 is the product NDC for Opsin II 6015 (opsin ii), Onion 3 [hp_X]/59mL + 11 more ingredients liquid, listed with the FDA by Professional Complementary Health Formulas. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Opsin II 6015 (Opsin II).
What is the active ingredient?: Onion, Ambrosia artemisiifolia whole, Euphrasia stricta, Wyethia helenioides root, Naphthalene, Epinephrine, Arundo pliniana root, Schoenocaulon officinale seed, Arsenic trioxide, Histamine dihydrochloride, Sodium chloride, Tobacco leaf.
Who is the labeler?: Professional Complementary Health Formulas, NDC labeler code 63083. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Opsin II 6015?: 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.

Opsin II 6015 (Opsin ii) NDC 63083-6015