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  4. NDC Product Code: 13411-862 Jba Verestor Mega Fiber Powder

NDC 13411-862 Jba Verestor Mega Fiber Powder

Vitamin C, Vitamin E, Inulin, Banana Stem Extract, Nattokinase, Houttuynia Cordata - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 13411-862?
  4. Active Ingredients
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. Pharmacologic Classes

Product Information

Get all the details for National Drug Code (NDC) 13411-862 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:
13411-862
Proprietary Name:
Jba Verestor Mega Fiber Powder
Non-Proprietary Name: [1]
Vitamin C, Vitamin E, Inulin, Banana Stem Extract, Nattokinase, Houttuynia Cordata Extract, Rutin, Beta-carotene
Substance Name: [2]
.alpha.-tocopherol; Ascorbic Acid; Banana; Beta Carotene; Houttuynia Cordata Top; Inulin; Nattokinase; Rutin
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler Name: [5]
Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals
Labeler Code:
13411
Product Label ID:
e7b861da-3851-4a75-b707-4a427c938ee1
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date: [9]
11-06-2024
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
Code Navigator:

Code Structure Chart

Product Details

What is NDC 13411-862?

The NDC code 13411-862 is assigned by the FDA to the product Jba Verestor Mega Fiber Powder which is a human over the counter drug product labeled by Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals. The generic name of Jba Verestor Mega Fiber Powder is vitamin c, vitamin e, inulin, banana stem extract, nattokinase, houttuynia cordata extract, rutin, beta-carotene. The product's dosage form is powder and is administered via oral form. The product is distributed in 2 packages with assigned NDC codes 13411-862-30 30 powder in 1 packet , 13411-862-60 60 powder in 1 packet . 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 Jba Verestor Mega Fiber Powder 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.
  • .ALPHA.-TOCOPHEROL 8 mg/1 - A natural tocopherol and one of the most potent antioxidant tocopherols. It exhibits antioxidant activity by virtue of the phenolic hydrogen on the 2H-1-benzopyran-6-ol nucleus. It has four methyl groups on the 6-chromanol nucleus. The natural d form of alpha-tocopherol is more active than its synthetic dl-alpha-tocopherol racemic mixture.
  • ASCORBIC ACID 100 mg/1 - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant.
  • BANANA 1000 mg/1
  • BETA CAROTENE 250 ug/1 - A carotenoid that is a precursor of VITAMIN A. Beta carotene is administered to reduce the severity of photosensitivity reactions in patients with erythropoietic protoporphyria (PORPHYRIA, ERYTHROPOIETIC).
  • HOUTTUYNIA CORDATA TOP 200 mg/1
  • INULIN 1500 mg/1 - A starch found in the tubers and roots of many plants. Since it is hydrolyzable to FRUCTOSE, it is classified as a fructosan. It has been used in physiologic investigation for determination of the rate of glomerular function.
  • NATTOKINASE 200 mg/1
  • RUTIN 25 mg/1 - A flavonol glycoside found in many plants, including BUCKWHEAT; TOBACCO; FORSYTHIA; HYDRANGEA; VIOLA, etc. It has been used therapeutically to decrease capillary fragility.

Which are Jba Verestor Mega Fiber Powder UNII Codes?

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

Which are Jba Verestor Mega Fiber Powder 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 Jba Verestor Mega Fiber Powder?

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".