Insta-char Aqueous Cherry
NDC 66689-202

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 66689-202?
  5. Insta-char Aqueous Cherry Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Patient Education

Product Information

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

Insta-char Aqueous Cherry is a OTC MONOGRAPH DRUG-approved product labeled by Vistapharm, Llc. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 66689-202 and 2 associated package configurations. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
66689-202
Proprietary Name:
Insta-char Aqueous Cherry
Product Type: [3]
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Vistapharm, Llc
Labeler Code:
66689
Product Label ID:
df1226cb-f2a8-4e91-b265-a08765f7683f
FDA Application Number: [6]
M023
Marketing Category: [8]
OTC MONOGRAPH DRUG

Marketing Timeline

Start Marketing Date: [9]
12-11-2007
End Marketing Date: [10]
05-31-2026
Listing Expiration Date: [11]
05-31-2026
Exclude Flag: [12]
D

Product Characteristics

Flavor(s):

Code Structure Chart

Product Details

What is NDC 66689-202?

The NDC code 66689-202 is assigned by the FDA to the product Insta-char Aqueous Cherry. This pharmaceutical product is labeled by Vistapharm, Llc and is currently categorized as listed product. In terms of distribution, this product is available in 2 different package configurations. The associated package NDC(s) include: 66689-202-04, 66689-202-08. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

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 to insert drinking straw included with bottle.Pull or cut off tip from included cherry flavor and squeeze flavor into straw.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, or health professional were unsuccessful, continue trying.Keep patient active and moving.Save the container of poison.AgeDoseChildren 1 t0 12 years old weighing at least 16kg (36 lbs.)Adults and children 12 years and over and weighing at least 32 kg (71 lbs.)15-30g activated charcoal or 1-2g per kg of body weight. If a second dose is recommended, the additional dose should be Insta-Char in an Aqueous Base unless otherwise directed by a physician.50 - 100 g (1-2 adult bottles) or 1-2 g per kg of body weight. If a second borrles is recommended, the additional bottle should be Insta-Char in an Aqueous Base unless otherwise directed by a physician.

Which are the associated UNII Codes?

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

Which are the Inactive Ingredients associated 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:

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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.
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* Please review the full disclaimer at the bottom of this page.

Product & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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.
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".