What is NDC 43742-1516?

43742-1516 is the product NDC for Electrolyte Plus, Boron citrate 6 [hp_X]/mL + 15 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 (Boron 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 Phosphorica).

What is the active ingredient?

Boron citrate, Calcium gluconate, Chromium picolinate, Cobaltous gluconate, Copper gluconate, Ferric chloride hexahydrate, Magnesium gluconate, Manganese gluconate, Potassium gluconate, Selenium dioxide, Sodium gluconate, Zinc gluconate, Dibasic potassium phosphate, Nickel, Vanadium, Tribasic calcium phosphate.

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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Electrolyte Plus NDC 43742-1516 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1516Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1516Add 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
43742-1516-1	4374215160143742151601	120 mL in 1 BOTTLE, DROPPER (43742-1516-1)Marketed from Aug 21, 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): Electrolyte Plus
Generic name (nonproprietary): boron 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 phosphorica
Active ingredients: Boron citrate — 6 [hp_X]/mLCalcium gluconate — 6 [hp_X]/mLChromium picolinate — 6 [hp_X]/mLCobaltous gluconate — 6 [hp_X]/mLCopper gluconate — 6 [hp_X]/mLFerric chloride hexahydrate — 6 [hp_X]/mLMagnesium gluconate — 6 [hp_X]/mLManganese gluconate — 6 [hp_X]/mLPotassium gluconate — 6 [hp_X]/mLSelenium dioxide — 6 [hp_X]/mLSodium gluconate — 6 [hp_X]/mLZinc gluconate — 6 [hp_X]/mLDibasic potassium phosphate — 8 [hp_X]/mLNickel — 8 [hp_X]/mLVanadium — 8 [hp_X]/mLTribasic calcium phosphate — 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: Aug 21, 2019
Marketing end: Mar 16, 2027
Other FDA classes: Allergens (Chemical structure)Calcium (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Divalent (Chemical structure)Cell-mediated Immunity (Physiologic effect)Decreased Copper Ion Absorption (Physiologic effect)Increased Coagulation Factor Activity (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)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Iron (Chemical structure)Magnesium Ion Exchange Activity (Mechanism)Magnetic Resonance Contrast Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Potassium Compounds (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 43742-1516_762c7ffb-6fc5-420f-972c-473a8169d92dSPL ID 762c7ffb-6fc5-420f-972c-473a8169d92dSPL set ID abeb996b-c754-4455-b4d4-eba514fdbcadUNII S043P4DV22, SQE6VB453K, S71T8B8Z6P, 26SK597UWV, RV823G6G67, 0I2XIN602U, T42NAD2KHC, 9YY2F980SV, 12H3K5QKN9, 9N3UK29E57, R6Q3791S76, U6WSN5SQ1Z, CI71S98N1Z, 7OV03QG267, 00J9J9XKDE, 91D9GV0Z28
Pharmacologic class: Blood Coagulation Factor; Calculi Dissolution Agent; Copper Absorption Inhibitor; Osmotic Laxative; Paramagnetic Contrast Agent; Parenteral Iron Replacement; Phosphate Binder; Potassium Salt; 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

N443742151601 followed by a unit qualifier and the quantity

Package 43742-1516-01. 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 Oct 11, 2023.

Indications (excerpt from the label)

HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms relating to electrolyte imbalance such as dizziness and fatigue.** **These statements are based upon traditional 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 43742-1516

What is NDC 43742-1516?: 43742-1516 is the product NDC for Electrolyte Plus, Boron citrate 6 [hp_X]/mL + 15 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 (Boron 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 Phosphorica).
What is the active ingredient?: Boron citrate, Calcium gluconate, Chromium picolinate, Cobaltous gluconate, Copper gluconate, Ferric chloride hexahydrate, Magnesium gluconate, Manganese gluconate, Potassium gluconate, Selenium dioxide, Sodium gluconate, Zinc gluconate, Dibasic potassium phosphate, Nickel, Vanadium, Tribasic calcium phosphate.
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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Electrolyte Pluskali 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	Potassium chloride 3 [hp_X]/mL + 22 more ingredients	LiquidOral	Deseret Biologicals, Inc.	43742-2082	43742-2082-01