NDC 43742-1516 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

NDC Product Code 43742-1516

NDC Code: 43742-1516

Proprietary Name: Electrolyte Plus What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: 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 Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-1516-1

Package Description: 120 mL in 1 BOTTLE, DROPPER

NDC Product Information

Electrolyte Plus with NDC 43742-1516 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Electrolyte Plus is 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. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Deseret Biologicals, Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Electrolyte Plus Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • BORON CITRATE 6 [hp_X]/mL
  • CALCIUM GLUCONATE 6 [hp_X]/mL
  • CHROMIUM PICOLINATE 6 [hp_X]/mL
  • COBALTOUS GLUCONATE 6 [hp_X]/mL
  • COPPER GLUCONATE 6 [hp_X]/mL
  • FERRIC CHLORIDE HEXAHYDRATE 6 [hp_X]/mL
  • MAGNESIUM GLUCONATE 6 [hp_X]/mL
  • MANGANESE GLUCONATE 6 [hp_X]/mL
  • POTASSIUM GLUCONATE 6 [hp_X]/mL
  • SELENIUM DIOXIDE 6 [hp_X]/mL
  • SODIUM GLUCONATE 6 [hp_X]/mL
  • ZINC GLUCONATE 6 [hp_X]/mL
  • DIBASIC POTASSIUM PHOSPHATE 8 [hp_X]/mL
  • NICKEL 8 [hp_X]/mL
  • VANADIUM 8 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 9 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ASCORBIC ACID (UNII: PQ6CK8PD0R)
  • DEXTROSE MONOHYDRATE (UNII: LX22YL083G)
  • ALCOHOL (UNII: 3K9958V90M)
  • ARGININE (UNII: 94ZLA3W45F)
  • LEVOCARNITINE (UNII: 0G389FZZ9M)
  • LEUCINE (UNII: GMW67QNF9C)
  • ORNITHINE (UNII: E524N2IXA3)
  • VALINE (UNII: HG18B9YRS7)
  • MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
  • GRAPE (UNII: 6X543N684K)
  • POTASSIUM CHLORIDE (UNII: 660YQ98I10)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Deseret Biologicals, Inc.
Labeler Code: 43742
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 08-21-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Electrolyte Plus Product Label Images

Electrolyte Plus Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Boron Citrate 6X, Calcium Gluconate 6X, Chromium Picolinate 6X, Cobalt Gluconate 6X, Copper Gluconate 6X, Ferrous Muriaticum 6X, Magnesium Gluconicum Dihydricum 6X, Manganese Gluconate 6X, Potassium Gluconate 6X, Selenium Dioxide 6X, Sodium Gluconate 6X, Zincum Gluconicum 6X, Kali Phosphoricum 8X, Niccolum Metallicum 8X, Vanadium Metallicum 8X, Calcarea Phosphorica 9X.

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.

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.

Warnings:

Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away.If pregnant or breast-feeding, seek advice of a health professional before use.Tamper seal: "Sealed for Your Protection."Do not use if seal is broken or missing.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away.

Directions:

1/2 tsp twice a day for stamina building and muscle recovery, best if taken 1/2 hour prior to workout. For more strenuous workouts dosage may be increased up to 1 tsp. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Ascorbic Acid, Demineralized Water, Dextrose Monohydrate, 12% Ethanol, L-Arginine, L-Carnitine, L-Leucine, L-Ornithine HCL, L-Valine, Magnesium Chloride, Organic Grape Flavored Syrup, Potassium Chloride, Sodium Chloride.

Questions:

Dist. by: Deseret Biologicals, Inc.469 W. Parkland DriveSandy, UT 84070 www.desbio.com

Package Label Display:

DESBIONDC 43742-1516-1HOMEOPATHICELECTROLYTEPLUS4 FL OZ (120 ml)

* Please review the disclaimer below.