What is NDC 43742-1571?

43742-1571 is the product NDC for Enviroclenz, Berberis vulgaris root bark 3 [hp_X]/mL + 24 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Enviroclenz (Berberis Vulgaris, Carduus Marianus, Chelidonium Majus, Glycyrrhiza Glabra, Lappa Major, Rhamnus Frangula, Stillingia Sylvatica, Taraxacum Officinale, Trifolium Pratense, Germanium Sesquioxide, Phytolacca Decandra, Acetone, Ammonium Muriaticum, Benzinum, Propylene Glycol, Sodium Lauryl Sulfate, Sodium Tripolyphosphate, Terebinthina, Methanol, Chlorinum, Iridium Metallicum, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Phosphoricum Acidum).

What is the active ingredient?

Berberis vulgaris root bark, Milk thistle, Chelidonium majus whole, Glycyrrhiza glabra, Arctium lappa root, Frangula alnus bark, Stillingia sylvatica root, Taraxacum officinale flowering top, Trifolium pratense leaf, Germanium sesquioxide, Phytolacca americana root, Acetone, Ammonium chloride, Benzene, Propylene glycol, Sodium lauryl sulfate, Sodium tripolyphosphate, Turpentine oil, Methyl alcohol, Chlorine, Iridium, Lycopodium clavatum spore, Nitric acid, Strychnos nux-vomica seed, Phosphoric acid.

Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Enviroclenz?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Enviroclenz NDC 43742-1571 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1571Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1571Add 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
43742-1571-1	4374215710143742157101	30 mL in 1 BOTTLE, DROPPER (43742-1571-1)Marketed from Sep 27, 2019

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): Enviroclenz
Generic name (nonproprietary): berberis vulgaris, carduus marianus, chelidonium majus, glycyrrhiza glabra, lappa major, rhamnus frangula, stillingia sylvatica, taraxacum officinale, trifolium pratense, germanium sesquioxide, phytolacca decandra, acetone, ammonium muriaticum, benzinum, propylene glycol, sodium lauryl sulfate, sodium tripolyphosphate, terebinthina, methanol, chlorinum, iridium metallicum, lycopodium clavatum, nitricum acidum, nux vomica, phosphoricum acidum
Active ingredients: Berberis vulgaris root bark — 3 [hp_X]/mLMilk thistle — 3 [hp_X]/mLChelidonium majus whole — 3 [hp_X]/mLGlycyrrhiza glabra — 3 [hp_X]/mLArctium lappa root — 3 [hp_X]/mLFrangula alnus bark — 3 [hp_X]/mLStillingia sylvatica root — 3 [hp_X]/mLTaraxacum officinale flowering top — 3 [hp_X]/mLTrifolium pratense leaf — 3 [hp_X]/mLGermanium sesquioxide — 8 [hp_X]/mLPhytolacca americana root — 8 [hp_X]/mLAcetone — 9 [hp_X]/mLAmmonium chloride — 9 [hp_X]/mLBenzene — 9 [hp_X]/mLPropylene glycol — 9 [hp_X]/mLSodium lauryl sulfate — 9 [hp_X]/mLSodium tripolyphosphate — 9 [hp_X]/mLTurpentine oil — 9 [hp_X]/mLMethyl alcohol — 9 [hp_X]/mLChlorine — 10 [hp_X]/mLIridium — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLNitric acid — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.NDC labeler code 43742
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 27, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (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)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 43742-1571_168569e6-610f-491b-81e3-0ff2ba1be972SPL ID 168569e6-610f-491b-81e3-0ff2ba1be972SPL set ID 92816bbe-96d6-45fc-9929-d3e6df394a33UNII 1TH8Q20J0U, U946SH95EE, 7E889U5RNN, 2788Z9758H, 597E9BI3Z3, S2D77IH61R, QBR70R4FBK, DQS85W46HV, 612YOZ36DG, 96WE91N25T, 11E6VI8VEG, 1364PS73AF, 01Q9PC255D, J64922108F, 6DC9Q167V3, 368GB5141J, 5HK03SA80J, C5H0QJ6V7F, Y4S76JWI15, 4R7X1O2820, 44448S9773, C88X29Y479, 411VRN1TV4, 269XH13919, E4GA8884NNUPC 0810151880600
Pharmacologic class: Non-Standardized Food Allergenic Extract; 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

N443742157101 followed by a unit qualifier and the quantity

Package 43742-1571-01. 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 May 2, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • toxicity support • neck pain • hives • cough • headache • occasional constipation 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)

About NDC 43742-1571

What is NDC 43742-1571?: 43742-1571 is the product NDC for Enviroclenz, Berberis vulgaris root bark 3 [hp_X]/mL + 24 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Enviroclenz (Berberis Vulgaris, Carduus Marianus, Chelidonium Majus, Glycyrrhiza Glabra, Lappa Major, Rhamnus Frangula, Stillingia Sylvatica, Taraxacum Officinale, Trifolium Pratense, Germanium Sesquioxide, Phytolacca Decandra, Acetone, Ammonium Muriaticum, Benzinum, Propylene Glycol, Sodium Lauryl Sulfate, Sodium Tripolyphosphate, Terebinthina, Methanol, Chlorinum, Iridium Metallicum, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Phosphoricum Acidum).
What is the active ingredient?: Berberis vulgaris root bark, Milk thistle, Chelidonium majus whole, Glycyrrhiza glabra, Arctium lappa root, Frangula alnus bark, Stillingia sylvatica root, Taraxacum officinale flowering top, Trifolium pratense leaf, Germanium sesquioxide, Phytolacca americana root, Acetone, Ammonium chloride, Benzene, Propylene glycol, Sodium lauryl sulfate, Sodium tripolyphosphate, Turpentine oil, Methyl alcohol, Chlorine, Iridium, Lycopodium clavatum spore, Nitric acid, Strychnos nux-vomica seed, Phosphoric acid.
Who is the labeler?: Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Enviroclenz?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.