Bacterial Nosode 4002 (bacterial nosode) NDC 63083-4002

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-4002Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-4002Add 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
63083-4002-2	63083400202	59 mL in 1 BOTTLE, DROPPER (63083-4002-2)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): Bacterial Nosode 4002Suffix: 4002
Generic name (nonproprietary): bacterial nosode
Active ingredients: Escherichia coli — 30 [hp_X]/59mLDiphtherial respiratory pseudomembrane human — 30 [hp_X]/59mLStreptococcus pyogenes — 30 [hp_X]/59mLProteus vulgaris — 30 [hp_X]/59mLRancid beef — 30 [hp_X]/59mLSalmonella enterica enterica serovar typhi — 30 [hp_X]/59mLJusticia spicigera leaf — 30 [hp_X]/59mLStaphylococcus aureus — 30 [hp_X]/59mLBovine tuberculin — 30 [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 63083-4002_a7331f8f-8e26-496a-91b4-9137c92b7af6SPL ID a7331f8f-8e26-496a-91b4-9137c92b7af6SPL set ID e363e251-2e86-4267-aff5-9c0e1ace774cUNII 514B9K0L10, 50SG618FGN, LJ2LP0YL98, 11T9HCO30O, 29SUH5R3HU, 760T5R8B3O, 2A6D37HK4A, O478WX4004, HKD62G79N5

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

N463083400202 followed by a unit qualifier and the quantity

Package 63083-4002-02. 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 Temporarily reduces occasional mild abdominal pain or discomfort, nausea, headache, fatigue, runny nose, chills, cough, congestion, or minor sore throat.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)