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  4. NDC Product Code: 82797-423 Enerjizer

NDC 82797-423 Enerjizer

Avena Sativa,Alfalfa,Echinacea,Ginkgo Biloba,Ginseng Panax,Caffeinum,Gentiana - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 82797-423?
  5. Enerjizer Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes
  9. Pharmacologic Classes

Product Information

Get all the details for National Drug Code (NDC) 82797-423 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
82797-423
Proprietary Name:
Enerjizer
Non-Proprietary Name: [1]
Avena Sativa, Alfalfa, Echinacea, Ginkgo Biloba, Ginseng Panax, Caffeinum, Gentiana Lut, Sterculia Acum, Calcium Phosphate, Chromium Oxide, Cobaltum Met, Cuprum Sulphuricum, Iodium, Lecithinum, Manganese Sulphate, Magnesium Oxide, Kali Muriaticum, Selenium, Zinc Sulphate
Substance Name: [2]
Alfalfa; Avena Sativa Whole; Basic Copper Sulfate; Caffeine; Calcium Phosphate; Chromic Oxide; Cobalt; Cola Acuminata Whole; Echinacea, Unspecified; Gentiana Lutea Whole; Ginkgo Biloba Whole; Iodine; Lecithin, Soybean; Magnesium Oxide; Manganese Sulfate; Panax Ginseng Whole; Potassium Chloride; Selenium; Zinc Sulfate
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler Name: [5]
Dr. Masood Homeopathic Pharmaceuticals Private Limited
Labeler Code:
82797
Product Label ID:
1d08ce52-0604-04d0-e063-6294a90a7412
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
07-15-2024
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332 - GOLDEN)
Shape:
OVAL (C48345)
Size(s):
5 MM
Score:
1

Code Structure Chart

Product Details

What is NDC 82797-423?

The NDC code 82797-423 is assigned by the FDA to the product Enerjizer which is a human over the counter drug product labeled by Dr. Masood Homeopathic Pharmaceuticals Private Limited. The generic name of Enerjizer is avena sativa, alfalfa, echinacea, ginkgo biloba, ginseng panax, caffeinum, gentiana lut, sterculia acum, calcium phosphate, chromium oxide, cobaltum met, cuprum sulphuricum, iodium, lecithinum, manganese sulphate, magnesium oxide, kali muriaticum, selenium, zinc sulphate. The product's dosage form is tablet, coated and is administered via oral form. The product is distributed in a single package with assigned NDC code 82797-423-30 30 mg in 1 blister pack . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Enerjizer?

Restores the lost vigour and vitality.Bad effects of prolonged illness.Mental fatigue or exhaustion.Acts as prophylactic against viral diseases.Lowers cholesterol and control glucose level in body.Reduce inflammation in body.Helpful in regulation of blood pressure and reduce fatigue.Keeps you energetic during exercise.Makes muscles stronger.Fulfill iodine deficiency and helpful in thyroid gland functioning.Prevents from cerebral thrombosis and stroke

What are Enerjizer Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
  • ALFALFA .11392 mg/660mg
  • AVENA SATIVA WHOLE .11392 mg/660mg
  • BASIC COPPER SULFATE .00128 mg/660mg
  • CAFFEINE .192 mg/660mg - A methylxanthine naturally occurring in some beverages and also used as a pharmacological agent. Caffeine's most notable pharmacological effect is as a central nervous system stimulant, increasing alertness and producing agitation. It also relaxes SMOOTH MUSCLE, stimulates CARDIAC MUSCLE, stimulates DIURESIS, and appears to be useful in the treatment of some types of headache. Several cellular actions of caffeine have been observed, but it is not entirely clear how each contributes to its pharmacological profile. Among the most important are inhibition of cyclic nucleotide PHOSPHODIESTERASES, antagonism of ADENOSINE RECEPTORS, and modulation of intracellular calcium handling.
  • CALCIUM PHOSPHATE .128 mg/660mg
  • CHROMIC OXIDE .00128 mg/660mg
  • COBALT .00128 mg/660mg - A trace element that is a component of vitamin B12. It has the atomic symbol Co, atomic number 27, and atomic weight 58.93. It is used in nuclear weapons, alloys, and pigments. Deficiency in animals leads to anemia; its excess in humans can lead to erythrocytosis.
  • COLA ACUMINATA WHOLE .0576 mg/660mg
  • ECHINACEA, UNSPECIFIED .0576 mg/660mg
  • GENTIANA LUTEA WHOLE .0576 mg/660mg
  • GINKGO BILOBA WHOLE .0128 mg/660mg
  • IODINE .0128 mg/660mg - A nonmetallic element of the halogen group that is represented by the atomic symbol I, atomic number 53, and atomic weight of 126.90. It is a nutritionally essential element, especially important in thyroid hormone synthesis. In solution, it has anti-infective properties and is used topically.
  • LECITHIN, SOYBEAN .064 mg/660mg
  • MAGNESIUM OXIDE .0128 mg/660mg - Magnesium oxide (MgO). An inorganic compound that occurs in nature as the mineral periclase. In aqueous media combines quickly with water to form magnesium hydroxide. It is used as an antacid and mild laxative and has many nonmedicinal uses.
  • MANGANESE SULFATE .0128 mg/660mg
  • PANAX GINSENG WHOLE .0128 mg/660mg
  • POTASSIUM CHLORIDE .0128 mg/660mg - A white crystal or crystalline powder used in BUFFERS; FERTILIZERS; and EXPLOSIVES. It can be used to replenish ELECTROLYTES and restore WATER-ELECTROLYTE BALANCE in treating HYPOKALEMIA.
  • SELENIUM .0032 mg/660mg - An element with the atomic symbol Se, atomic number 34, and atomic weight 78.97. It is an essential micronutrient for mammals and other animals but is toxic in large amounts. Selenium protects intracellular structures against oxidative damage. It is an essential component of GLUTATHIONE PEROXIDASE.
  • ZINC SULFATE .0192 mg/660mg - A compound given in the treatment of conditions associated with zinc deficiency such as acrodermatitis enteropathica. Externally, zinc sulfate is used as an astringent in lotions and eye drops. (Reynolds JEF(Ed): Martindale: The Extra Pharmacopoeia (electronic version). Micromedex, Inc, Englewood, CO, 1995)

Which are Enerjizer UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Enerjizer Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

Which are the Pharmacologic Classes for Enerjizer?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

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Product Footnotes

[1] 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.

[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

[3] 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.

[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

[8] 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.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".