West Parasite Detox 6039 (west parasite detox) NDC 63083-6039

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-6039Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-6039Add 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
63083-6039-2	63083603902	59 mL in 1 BOTTLE, DROPPER (63083-6039-2)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): West Parasite Detox 6039Suffix: 6039
Generic name (nonproprietary): west parasite detox
Active ingredients: Ancylostoma duodenale — 30 [hp_X]/59mLAscaris lumbricoides — 30 [hp_X]/59mLBlastocystis hominis — 30 [hp_X]/59mLCryptosporidium hominis — 30 [hp_X]/59mLDientamoeba fragilis — 30 [hp_X]/59mLEchinococcus granulosus — 30 [hp_X]/59mLEntamoeba histolytica — 30 [hp_X]/59mLEnterococcus faecium — 30 [hp_X]/59mLWuchereria bancrofti — 30 [hp_X]/59mLGiardia lamblia — 30 [hp_X]/59mLEnterobius vermicularis — 30 [hp_X]/59mLPlasmodium knowlesi — 30 [hp_X]/59mLBandtooth conger — 30 [hp_X]/59mLTrichomonas vaginalis — 30 [hp_X]/59mLTrichinella spiralis — 30 [hp_X]/59mLToxoplasma gondii — 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 63083-6039_5b6ce891-275b-4623-a7d0-edaec38015ebSPL ID 5b6ce891-275b-4623-a7d0-edaec38015ebSPL set ID d0e4d793-89b7-4cde-afba-443cf5e1307dUNII 84H4A6227O, 5694HE17ZQ, 66KX72J4H6, DKE8M34J72, W1WFA6001P, D0396L455U, 2XC2HJ478W, 34YYS7G16P, 7OR5YIL2C6, 89IEJ09R73, W1D68QW48M, 0LFT87M341, 4L1B1DW0X8, Q25X3G314L, 2PYI6D7HCQ, BMV90JF469

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

N463083603902 followed by a unit qualifier and the quantity

Package 63083-6039-02. 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 mild abdominal pain, nausea or vomiting, diarrhea, coughing or wheezing, difficulty breathing, fatigue, or feelings of discomfort or uneasiness.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)