Enviro Detox Formula NDC 83027-0120

NDC codes

FDA NDC Directory

Product NDC (as listed)83027-0120Labeler and product segments. Claims need a package NDC.

Product NDC at billing width83027-0120Add 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
83027-0120-1	83027012001	60 mL in 1 BOTTLE, SPRAY (83027-0120-1)Marketed from Oct 6, 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): Enviro Detox Formula
Generic name (nonproprietary): lappa major, taraxacum officinale, trifolium pratense, spinacia, petroleum, plumbum metallicum, sulphuricum acidum, ammonium phosphoricum, arsenicum album, chromium (metallicum), cuprum metallicum, dibromoethane, kreosotum, mercurius vivus, mtbe (tert-butyl methyl ether), nitricum acidum, radium bromatum
Active ingredients: Arctium lappa root — 3 [hp_X]/mLTaraxacum officinale — 3 [hp_X]/mLTrifolium pratense flower — 3 [hp_X]/mLSpinacia oleracea root — 6 [hp_X]/mLKerosene — 12 [hp_X]/mLLead — 12 [hp_X]/mLSulfuric acid — 12 [hp_X]/mLAmmonium phosphate, Dibasic — 30 [hp_X]/mLArsenic trioxide — 30 [hp_X]/mLChromium — 30 [hp_X]/mLCopper — 30 [hp_X]/mLEthylene dibromide — 30 [hp_X]/mLWood creosote — 30 [hp_X]/mLMercury — 30 [hp_X]/mLTert-butyl methyl ether — 30 [hp_X]/mLNitric acid — 30 [hp_X]/mLRadium bromide — 30 [hp_X]/mL
Dosage form: Spray
Route: Oral
Labeler: Nutritional Specialties, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 6, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Increased Histamine Release (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)
Identifiers: Product ID 83027-0120_21c70f99-2a67-415b-baea-9d46016850faSPL ID 21c70f99-2a67-415b-baea-9d46016850faSPL set ID 83825312-dff8-4caa-8afa-bb1eab7397f7UNII 597E9BI3Z3, 39981FM375, 4JS0838828, A19RZC6BEH, 1C89KKC04E, 2P299V784P, O40UQP6WCF, 10LGE70FSU, S7V92P67HO, 0R0008Q3JB, 789U1901C5, 1N41638RNO, 3JYG22FD73, FXS1BY2PGL, 29I4YB3S89, 411VRN1TV4, R74O7T8569UPC 0649818024091
Pharmacologic class: Copper-containing Intrauterine Device; Standardized Chemical Allergen

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

N483027012001 followed by a unit qualifier and the quantity

Package 83027-0120-01. 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

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