Pollutox NDC 43742-2095

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-2095Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-2095Add 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
43742-2095-1	43742209501	30 mL in 1 BOTTLE, DROPPER (43742-2095-1)Marketed from Oct 13, 2023

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): Pollutox
Generic name (nonproprietary): sulphuricum acidum, berberis vulgaris, arsenicum album, benzinum, cadmium sulphuratum, hydrofluoricum acidum, melatonin, nitrogenum oxygenatum, nux vomica, petroleum, plumbum metallicum, stannum metallicum, toluene, acetone, carbon dioxide, chlorinum, mercurius solubilis, ozone, uranium nitricum
Active ingredients: Sulfuric acid — 6 [hp_X]/mLBerberis vulgaris root bark — 8 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLBenzene — 12 [hp_X]/mLCadmium sulfide — 12 [hp_X]/mLHydrofluoric acid — 12 [hp_X]/mLMelatonin — 12 [hp_X]/mLNitrous oxide — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLKerosene — 12 [hp_X]/mLLead — 12 [hp_X]/mLTin — 12 [hp_X]/mLToluene — 12 [hp_X]/mLAcetone — 12 [hp_X]/mLCarbon dioxide — 12 [hp_X]/mLChlorine — 12 [hp_X]/mLMercurius solubilis — 12 [hp_X]/mLOzone — 16 [hp_X]/mLUranyl nitrate hexahydrate — 15 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 13, 2023
Marketing end: Jul 17, 2029
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)X-Ray Contrast Activity (Mechanism)
Identifiers: Product ID 43742-2095_adde01c6-2ac7-4f44-9cb9-082cf8c7b0cbSPL ID adde01c6-2ac7-4f44-9cb9-082cf8c7b0cbSPL set ID e7000300-69ec-47db-8059-3f873d64f177UNII O40UQP6WCF, 1TH8Q20J0U, S7V92P67HO, J64922108F, 057EZR4Z7Q, RGL5YE86CZ, JL5DK93RCL, K50XQU1029, 269XH13919, 1C89KKC04E, 2P299V784P, 387GMG9FH5, 3FPU23BG52, 1364PS73AF, 142M471B3J, 4R7X1O2820, 324Y4038G2, 66H7ZZK23N, 3V057702FYUPC 0810151883687
Pharmacologic class: Non-Standardized Plant Allergenic Extract; Radiographic Contrast Agent

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

N443742209501 followed by a unit qualifier and the quantity

Package 43742-2095-01. 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 Jul 31, 2026.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • nausea • fatigue • head pain • abdominal pain These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)