What is NDC 63083-9415?

63083-9415 is the product NDC for Proteus Nosode Combination 9415 (proteus nosode combination), Gelsemium sempervirens root 3 [hp_X]/29.5mL + 5 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?

Proteus Nosode Combination 9415 (Proteus Nosode Combination).

What is the active ingredient?

Gelsemium sempervirens root, Colchicum autumnale bulb, Citrullus colocynthis fruit pulp, Strychnos nux-vomica seed, Proteus inconstans, Mercuric chloride.

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 Proteus Nosode Combination 9415?

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.

Proteus Nosode Combination 9415 NDC 63083-9415

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-9415Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-9415Add 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
63083-9415-1	6308394150163083941501	29.5 mL in 1 BOTTLE, DROPPER (63083-9415-1)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): Proteus Nosode Combination 9415Suffix: 9415
Generic name (nonproprietary): proteus nosode combination
Active ingredients: Gelsemium sempervirens root — 3 [hp_X]/29.5mLColchicum autumnale bulb — 4 [hp_X]/29.5mLCitrullus colocynthis fruit pulp — 6 [hp_X]/29.5mLStrychnos nux-vomica seed — 6 [hp_X]/29.5mLProteus inconstans — 12 [hp_X]/29.5mLMercuric chloride — 12 [hp_X]/29.5mL
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: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 63083-9415_41d6f2e3-f0db-4447-91fb-53bc3c25e3fbSPL ID 41d6f2e3-f0db-4447-91fb-53bc3c25e3fbSPL set ID 6436f103-d155-4d60-8ccb-a4514c5d0ebdUNII 639KR60Q1Q, 993QHL78E6, 23H32AOH17, 269XH13919, UTX536WN6N, 53GH7MZT1R
Pharmacologic class: Non-Standardized Plant Allergenic Extract

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

N463083941501 followed by a unit qualifier and the quantity

Package 63083-9415-01. 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 urinary discomfort, difficulty or increased frequency, minor back pain, fatigue, nausea, vomiting, or diarrhea.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-9415

What is NDC 63083-9415?: 63083-9415 is the product NDC for Proteus Nosode Combination 9415 (proteus nosode combination), Gelsemium sempervirens root 3 [hp_X]/29.5mL + 5 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?: Proteus Nosode Combination 9415 (Proteus Nosode Combination).
What is the active ingredient?: Gelsemium sempervirens root, Colchicum autumnale bulb, Citrullus colocynthis fruit pulp, Strychnos nux-vomica seed, Proteus inconstans, Mercuric chloride.
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 Proteus Nosode Combination 9415?: 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.

Proteus Nosode Combination 9415 (Proteus nosode combination) NDC 63083-9415