Tap Water Detox 6018 (tap water detox) NDC 63083-6018

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-6018Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-6018Add 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
63083-6018-2	63083601802	59 mL in 1 BOTTLE, DROPPER (63083-6018-2)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): Tap Water Detox 6018Suffix: 6018
Generic name (nonproprietary): tap water detox
Active ingredients: 2,3,7,8-tetrachlorodibenzo-p-dioxin — 60 [hp_X]/59mLBromine — 30 [hp_X]/59mLChlorine — 30 [hp_X]/59mLChloroform — 30 [hp_X]/59mLCopper — 30 [hp_X]/59mLFluoride ion — 30 [hp_X]/59mLIron — 30 [hp_X]/59mLLead — 30 [hp_X]/59mLSodium fluoride — 30 [hp_X]/59mLPhenol — 30 [hp_X]/59mLPentaerythritol tetrakis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate) — 30 [hp_X]/59mLFenson — 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
Other FDA classes: Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)
Identifiers: Product ID 63083-6018_733a04a4-7c26-4a42-bd4e-5bb2083eacf9SPL ID 733a04a4-7c26-4a42-bd4e-5bb2083eacf9SPL set ID ae0bca6a-118e-40a2-9108-14fc41552444UNII DO80M48B6O, SBV4XY874G, 4R7X1O2820, 7V31YC746X, 789U1901C5, Q80VPU408O, E1UOL152H7, 2P299V784P, 8ZYQ1474W7, 339NCG44TV, 255PIF62MS, DFC2HB4I0K
Pharmacologic class: Copper-containing Intrauterine Device

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

N463083601802 followed by a unit qualifier and the quantity

Package 63083-6018-02. 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, shortness of breath, minor rash or itchy skin, or occasional headache due to sensitivity to or exposure to common tap water additives or contaminants.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)