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  4. NDC Product Code: 66689-201 Insta-char Aqueous

NDC 66689-201 Insta-char Aqueous

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 66689-201?
  4. Insta-char Aqueous Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Get all the details for National Drug Code (NDC) 66689-201 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:
66689-201
Proprietary Name:
Insta-char Aqueous
Product Type: [3]
Labeler Name: [5]
Vistapharm, Llc
Labeler Code:
66689
Product Label ID:
2938dd7e-1f32-48be-bc91-56c6bf9c8aac
FDA Application Number: [6]
M023
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
10-03-2006
End Marketing Date: [10]
08-31-2025
Listing Expiration Date: [11]
08-31-2025
Exclude Flag: [12]
D
Code Navigator:

Code Structure Chart

Product Details

What is NDC 66689-201?

The NDC code 66689-201 is assigned by the FDA to the product Insta-char Aqueous which is product labeled by Vistapharm, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 66689-201-08 240 ml in 1 bottle, plastic . 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 Insta-char Aqueous?

Shake vigorously to suspend charcoal before use.Remove foil seal underneath cap and replace cap.Cut off delivery tip of bottle 3/4 inch from end for drinking.Administer entire 240 mL if possible.Repeat dose immediately with Insta-Char Aqueous base product if possible.If previous attempts to contact a poison control center, emergency medical facility, of health professional were unsuccessful, continue trying.Keep patient active and moving.Save the container of poison.AgeDoseAdult and Children 12 years and over and weighing at least 32 kg (71 lbs.)50-100g (1-2 adult bottles) or 1-2g per kg of body weight. If a second bottle is recommended, the additional bottle should be Insta-Char in an Aqueous Base unless otherwise directed by a physician.

Which are Insta-char Aqueous UNII Codes?

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

Which are Insta-char Aqueous 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:

* Please review the disclaimer below.

Patient Education

Activated Charcoal


What is it? Activated charcoal has pores that can trap chemicals. It is typically taken by mouth as a treatment for some swallowed poisons. There is little evidence for other uses.

Charcoal is made from peat, coal, wood, coconut shell, or petroleum. Activated charcoal is made by heating charcoal in the presence of a gas. This process causes the charcoal to develop lots of internal spaces or pores. These pores help activated charcoal trap chemicals.

Activated charcoal is commonly used to treat poisoning. It is also used for high cholesterol, hangovers, and upset stomach, but there is no strong scientific evidence to support most of these uses.
[Learn More]


* Please review the disclaimer below.

Product Footnotes

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

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[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.

[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

[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".