Energy Catalyst NDC 43742-2203

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-2203Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-2203Add 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
43742-2203-1	43742220301	60 mL in 1 BOTTLE, DROPPER (43742-2203-1)Marketed from Dec 10, 2024

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): Energy Catalyst
Generic name (nonproprietary): adenosinum cyclophosphoricum, alumina, arsenicum album, cerium oxalicum, cobalt gluconate, cuprum sulphuricum, calcarea phosphorica, chromium metallicum, cobaltum metallicum, cuprum metallicum, ferrum metallicum, iodium, iridium metallicum, kali carbonicum, lithium carbonicum, magnesium metallicum, manganum metallicum, molybdenum, natrum muriaticum, phosphorus, selenium metallicum, strontium carbonicum, sulphur, vanadium metallicum, zincum metallicum, aluminium metallicum, antimonium crudum,
Active ingredients: Adenosine cyclic phosphate — 8 [hp_X]/mLAluminum oxide — 30 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLCerous oxalate nonahydrate — 8 [hp_X]/mLCobaltous gluconate — 6 [hp_X]/mLCupric sulfate — 6 [hp_X]/mLTribasic calcium phosphate — 8 [hp_X]/mLChromium — 8 [hp_X]/mLCobalt — 8 [hp_X]/mLCopper — 8 [hp_X]/mLIron — 8 [hp_X]/mLIodine — 8 [hp_X]/mLIridium — 8 [hp_X]/mLPotassium carbonate — 8 [hp_X]/mLLithium carbonate — 8 [hp_X]/mLMagnesium — 8 [hp_X]/mLManganese — 8 [hp_X]/mLMolybdenum — 8 [hp_X]/mLSodium chloride — 8 [hp_X]/mLPhosphorus — 6 [hp_X]/mLSelenium — 8 [hp_X]/mLStrontium carbonate — 8 [hp_X]/mLSulfur — 8 [hp_X]/mLVanadium — 8 [hp_X]/mLZinc — 8 [hp_X]/mLAluminum — 12 [hp_X]/mLAntimony trisulfide — 12 [hp_X]/mLSilver — 12 [hp_X]/mLGold — 12 [hp_X]/mLBarium carbonate — 12 [hp_X]/mLBeryllium — 12 [hp_X]/mLBismuth — 12 [hp_X]/mLBromine — 12 [hp_X]/mLCadmium — 12 [hp_X]/mLCerium — 12 [hp_X]/mLCesium chloride — 12 [hp_X]/mLDysprosium — 12 [hp_X]/mLErbium — 12 [hp_X]/mLEuropium — 12 [hp_X]/mLGadolinium — 12 [hp_X]/mLGermanium sesquioxide — 12 [hp_X]/mLHolmium — 12 [hp_X]/mLIndium — 12 [hp_X]/mLMercurius solubilis — 12 [hp_X]/mLNeodymium oxide — 12 [hp_X]/mLNickel — 12 [hp_X]/mLOsmium — 12 [hp_X]/mLPalladium — 12 [hp_X]/mLPlatinum — 12 [hp_X]/mLLead — 12 [hp_X]/mLPraseodymium — 12 [hp_X]/mLRhodium — 12 [hp_X]/mLRubidium nitrite — 12 [hp_X]/mLSamarium — 12 [hp_X]/mLTin — 12 [hp_X]/mLTerbium — 12 [hp_X]/mLThallium — 12 [hp_X]/mLYtterbium oxide — 12 [hp_X]/mLFerrous fumarate — 6 [hp_X]/mLLanthanum — 14 [hp_C]/mLMagnesium aspartate — 6 [hp_X]/mLManganese gluconate — 6 [hp_X]/mLMercuric chloride — 30 [hp_X]/mLNickel acetate — 8 [hp_X]/mLNiobium — 30 [hp_C]/mLPotassium aspartate — 6 [hp_X]/mLProteus morganii — 30 [hp_C]/mLSodium molybdate — 6 [hp_X]/mLTantalum — 30 [hp_C]/mLUranyl nitrate hexahydrate — 15 [hp_C]/mLViscum album fruiting top — 3 [hp_X]/mLCholecalciferol — 8 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 10, 2024
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Increased Coagulation Factor Activity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Magnetic Resonance Contrast Activity (Mechanism)Osmotic Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)Vitamin D (Chemical structure)
Identifiers: Product ID 43742-2203_1423f6de-22de-4a3a-8efc-63719246db02SPL ID 1423f6de-22de-4a3a-8efc-63719246db02
Pharmacologic class: Blood Coagulation Factor; Calculi Dissolution Agent; Copper-containing Intrauterine Device; Mood Stabilizer; Osmotic Laxative; Paramagnetic Contrast Agent; Phosphate Binder; Standardized Chemical Allergen; Vitamin D

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

N443742220301 followed by a unit qualifier and the quantity

Package 43742-2203-01. 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

The FDA listing for this product does not reference a label (SPL) set.