Industriox 6011 (industriox) NDC 63083-6011

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-6011Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-6011Add 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
63083-6011-2	63083601102	59 mL in 1 BOTTLE, DROPPER (63083-6011-2)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): Industriox 6011Suffix: 6011
Generic name (nonproprietary): industriox
Active ingredients: Berberis vulgaris root bark — 3 [hp_X]/59mLTaraxacum officinale — 3 [hp_X]/59mLAmmonium cation — 6 [hp_X]/59mLCamphor (Natural) — 6 [hp_X]/59mLStrychnos nux-vomica seed — 6 [hp_X]/59mLSulfuric acid — 6 [hp_X]/59mLOyster shell calcium carbonate, Crude — 12 [hp_X]/59mLLachesis muta venom — 12 [hp_X]/59mLLead — 12 [hp_X]/59mLAcetone — 30 [hp_X]/59mLAcrylic acid — 30 [hp_X]/59mLBenzene — 30 [hp_X]/59mLCarbon tetrachloride — 30 [hp_X]/59mLChloroform — 30 [hp_X]/59mLMethyl ethyl ketone — 30 [hp_X]/59mLFormaldehyde solution — 30 [hp_X]/59mLTert-butyl methyl ether — 30 [hp_X]/59mLNaphthalene — 30 [hp_X]/59mLLiquid petroleum — 30 [hp_X]/59mLTrichloroethylene — 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: 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 63083-6011_ef910ff0-f6b2-40ce-81d8-230a4c6a795eSPL ID ef910ff0-f6b2-40ce-81d8-230a4c6a795eSPL set ID ff4e04ce-6bff-419b-bb6b-d5e97b994283UNII 1TH8Q20J0U, 39981FM375, 54S68520I4, N20HL7Q941, 269XH13919, O40UQP6WCF, 2E32821G6I, VSW71SS07I, 2P299V784P, 1364PS73AF, J94PBK7X8S, J64922108F, CL2T97X0V0, 7V31YC746X, 6PT9KLV9IO, T0H3L6C7I5, 29I4YB3S89, 2166IN72UN, 6ZAE7X688J, 290YE8AR51
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

N463083601102 followed by a unit qualifier and the quantity

Package 63083-6011-02. 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 fatigue, lethargy, headaches, muscle or joint pain, mild bloating or gas, disturbed sleep, or lack of concentration due to sensitivity to or exposure to industrial chemicals, paint, petroleum, steel, and plastics.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)