Lawn and Garden Detox 6026 NDC 63083-6026

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-6026Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-6026Add 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
63083-6026-2	63083602602	59 mL in 1 BOTTLE, DROPPER (63083-6026-2)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): Lawn and Garden Detox 6026Suffix: 6026
Generic name (nonproprietary): lawn and garden detox
Active ingredients: 2-mercaptoethanol — 30 [hp_X]/59mLCarbon monoxide — 30 [hp_X]/59mLBorosilicate glass — 30 [hp_X]/59mLPolyvinyl alcohol, Unspecified — 30 [hp_X]/59mLMcpa — 30 [hp_X]/59mLEthyl butylacetylaminopropionate — 30 [hp_X]/59mLTralomethrin — 30 [hp_X]/59mLHops oil — 30 [hp_X]/59mLTitanium dioxide — 30 [hp_X]/59mLLiquid petroleum — 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 63083-6026_0ac4b569-715b-48ab-b798-98fc3938545fSPL ID 0ac4b569-715b-48ab-b798-98fc3938545fSPL set ID 2db4bdd8-1049-450a-8642-0e1dbbe5abb3UNII 14R9K67URN, 7U1EE4V452, BOJ6T9AR90, 532B59J990, D888C394VO, 65GQA237EH, W2Z59VSQ0O, 06JI9W529S, 15FIX9V2JP, 6ZAE7X688J

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

N463083602602 followed by a unit qualifier and the quantity

Package 63083-6026-02. 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 eye, nose, or throat irritation, occasional headache, coughing, shortness of breath, fatigue, or red, itchy, irritated skin due to sensitivity to or exposure to yard maintenance chemicals or materials.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)