NDC codes

FDA NDC Directory
Product NDC (as listed)43742-2082Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43742-2082Add 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
43742-2082-14374220820143742208201120 mL in 1 BOTTLE, DROPPER (43742-2082-1)Marketed from Oct 10, 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)
Electrolyte Plus
Generic name (nonproprietary)
kali muriaticum, l-arginine, l-carnitine, l-leucine, l-ornithine, l-valine, magnesia muriatica, ascorbicum acidum, borax, chromium oxydatum, ferrum muriaticum, kali carbonicum, magnesium gluconicum dihydricum, natrum muriaticum, zincum gluconicum, cuprum metallicum, kali phosphoricum, niccolum metallicum, selenium metallicum, vanadium metallicum, calcarea carbonica, calcarea phosphorica, manganum carbonicum
Active ingredients
Potassium chloride — 3 [hp_X]/mLArginine — 3 [hp_X]/mLLevocarnitine — 3 [hp_X]/mLLeucine — 3 [hp_X]/mLOrnithine — 3 [hp_X]/mLValine — 3 [hp_X]/mLMagnesium chloride — 3 [hp_X]/mLAscorbic acid — 6 [hp_X]/mLSodium borate — 6 [hp_X]/mLChromic oxide — 6 [hp_X]/mLFerric chloride hexahydrate — 6 [hp_X]/mLPotassium carbonate — 6 [hp_X]/mLMagnesium gluconate — 6 [hp_X]/mLSodium chloride — 6 [hp_X]/mLZinc gluconate — 6 [hp_X]/mLCopper — 8 [hp_X]/mLDibasic potassium phosphate — 8 [hp_X]/mLNickel — 8 [hp_X]/mLSelenium — 8 [hp_X]/mLVanadium — 8 [hp_X]/mLOyster shell calcium carbonate, Crude — 9 [hp_X]/mLTribasic calcium phosphate — 9 [hp_X]/mLManganese carbonate — 9 [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
Listing expires
Other FDA classes
Allergens (Chemical structure)Ascorbic Acid (Chemical structure)Calcium (Chemical structure)Carnitine (Chemical structure)Divalent (Chemical structure)Cell-mediated Immunity (Physiologic effect)Copper (Chemical structure)Decreased Copper Ion Absorption (Physiologic effect)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Increased Coagulation Factor Activity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Iron (Chemical structure)Magnesium Ion Exchange Activity (Mechanism)Magnesium Ion Exchange Activity (Mechanism)Magnetic Resonance Contrast Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Potassium Compounds (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers
Product ID 43742-2082_6d8759fc-72ad-4184-8586-f79d5ae9c844SPL ID 6d8759fc-72ad-4184-8586-f79d5ae9c844SPL set ID e3564733-8b88-4753-9077-9d74004d8ec9UNII 660YQ98I10, 94ZLA3W45F, 0G389FZZ9M, GMW67QNF9C, E524N2IXA3, HG18B9YRS7, 02F3473H9O, PQ6CK8PD0R, 91MBZ8H3QO, X5Z09SU859, 0I2XIN602U, BQN1B9B9HA, T42NAD2KHC, 451W47IQ8X, U6WSN5SQ1Z, 789U1901C5, CI71S98N1Z, 7OV03QG267, H6241UJ22B, 00J9J9XKDE, 2E32821G6I, 91D9GV0Z28, 9ZV57512ZMUPC 0810151881225
Pharmacologic class
Blood Coagulation Factor; Calculi Dissolution Agent; Carnitine Analog; Copper Absorption Inhibitor; Copper-containing Intrauterine Device; Osmotic Laxative; Paramagnetic Contrast Agent; Parenteral Iron Replacement; Phosphate Binder; Potassium Salt; Standardized Chemical Allergen; Vitamin C

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

N443742208201 followed by a unit qualifier and the quantity

Package 43742-2082-01. 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 .

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • dizziness • fatigue 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 43742-2082

What is NDC 43742-2082?
43742-2082 is the product NDC for Electrolyte Plus, Potassium chloride 3 [hp_X]/mL + 22 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?
Electrolyte Plus (Kali Muriaticum, L-Arginine, L-Carnitine, L-Leucine, L-Ornithine, L-Valine, Magnesia Muriatica, Ascorbicum Acidum, Borax, Chromium Oxydatum, Ferrum Muriaticum, Kali Carbonicum, Magnesium Gluconicum Dihydricum, Natrum Muriaticum, Zincum Gluconicum, Cuprum Metallicum, Kali Phosphoricum, Niccolum Metallicum, Selenium Metallicum, Vanadium Metallicum, Calcarea Carbonica, Calcarea Phosphorica, Manganum Carbonicum).
What is the active ingredient?
Potassium chloride, Arginine, Levocarnitine, Leucine, Ornithine, Valine, Magnesium chloride, Ascorbic acid, Sodium borate, Chromic oxide, Ferric chloride hexahydrate, Potassium carbonate, Magnesium gluconate, Sodium chloride, Zinc gluconate, Copper, Dibasic potassium phosphate, Nickel, Selenium, Vanadium, Oyster shell calcium carbonate, Crude, Tribasic calcium phosphate, Manganese carbonate.
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 Electrolyte Plus?
1 other product NDC are listed under this name. See all Electrolyte Plus NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Electrolyte Plus NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Electrolyte Plusboron citrate, calcium gluconate, chromium picolinate, cobalt gluconate, copper gluconate, ferrous muriaticum, magnesium gluconicum dihydricum, manganese gluconate, potassium gluconate, selenium dioxide, sodium gluconate, zincum gluconicum, kali phosphoricum, niccolum metallicum, vanadium metallicum, calcarea phosphoricaBoron citrate 6 [hp_X]/mL + 15 more ingredientsLiquidOralDeseret Biologicals, Inc.43742-151643742-1516-01

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