NDC codes

FDA NDC Directory
Product NDC (as listed)63083-6035Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63083-6035Add 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 NDC11-digit (billing)PackageCopy
63083-6035-26308360350259 mL in 1 BOTTLE, DROPPER (63083-6035-2)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)
Toxagent Detox 6035Suffix: 6035
Generic name (nonproprietary)
toxagent detox
Active ingredients
Chlorine — 12 [hp_X]/59mLChloroform — 12 [hp_X]/59mLFluorine — 12 [hp_X]/59mLMethane — 12 [hp_X]/59mLPhosfolan — 12 [hp_X]/59mLSulfur — 12 [hp_X]/59mLApis mellifera — 12 [hp_X]/59mLOnion — 30 [hp_X]/59mLAmmonium cation — 30 [hp_X]/59mLArsenic trioxide — 30 [hp_X]/59mLDieffenbachia seguine whole — 30 [hp_X]/59mLNitric acid — 30 [hp_X]/59mLFenson — 30 [hp_X]/59mLPropane — 30 [hp_X]/59mLSulfuric acid — 30 [hp_X]/59mLVeratrum album root — 30 [hp_X]/59mLCalendula officinalis flowering top — 30 [hp_X]/59mL2,3,7,8-tetrachlorodibenzo-p-dioxin — 60 [hp_X]/59mLAconitum napellus whole — 200 [hp_X]/59mLArnica montana whole — 200 [hp_X]/59mLBenzene — 200 [hp_X]/59mLHydrogen cyanide — 200 [hp_X]/59mLPotassium cyanide — 200 [hp_X]/59mL
Dosage form
Liquid
Route
Oral
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Allergens (Chemical structure)Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers
Product ID 63083-6035_67dc0d65-a899-4660-85e7-2a96f8735123SPL ID 67dc0d65-a899-4660-85e7-2a96f8735123SPL set ID e1476ce1-32ff-4c25-a330-dc78908f5591UNII 4R7X1O2820, 7V31YC746X, 284SYP0193, OP0UW79H66, CHJ98J84AY, 70FD1KFU70, 7S82P3R43Z, 492225Q21H, 54S68520I4, S7V92P67HO, 01800C6E6B, 411VRN1TV4, DFC2HB4I0K, T75W9911L6, O40UQP6WCF, QNS6W5US1Z, 18E7415PXQ, DO80M48B6O, U0NQ8555JD, O80TY208ZW, J64922108F, 2WTB3V159F, MQD255M2ZO
Pharmacologic class
Non-Standardized Food Allergenic Extract; Osmotic Laxative; Potassium Salt; Standardized Insect Venom 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

N463083603502 followed by a unit qualifier and the quantity

Package 63083-6035-02. 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 .

Indications (excerpt from the label)

INDICATIONS For the temporary relief of irritation of the nose, throat, eyes, or skin, occasional headache, shortness of breath, or fatigue due to sensitivity to or exposure to industrial processes or environmental contaminants.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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