Insta-char Aqueous
Poison Treatment Adsorbent
Vistapharm Inc
Human Otc Drug
NDC 66689-201Insta-char Aqueous also known as Poison Treatment Adsorbent is a human otc drug labeled by 'Vistapharm Inc'. National Drug Code (NDC) number for Insta-char Aqueous is 66689-201. This drug is available in dosage form of Suspension. The names of the active, medicinal ingredients in Insta-char Aqueous drug includes Activated Charcoal - 50 g/240mL . The currest status of Insta-char Aqueous drug is Active.
Drug Information:
| Drug NDC: | 66689-201 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Insta-char Aqueous |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Poison Treatment Adsorbent |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Vistapharm Inc |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Suspension |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | ACTIVATED CHARCOAL - 50 g/240mL
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | ORAL
|
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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. |
| Marketing Start Date: | 03 Oct, 2006 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 13 May, 2026 |
| 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. |
| Application Number: | part357 |
| 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. |
| Listing Expiration Date: | 31 Dec, 2023 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | VISTAPHARM INC
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 212227
309150
|
| The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UPC: | 0066689201084
|
| UPC stands for Universal Product Code. |
| UNII: | 2P3VWU3H10
|
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 66689-201-08 | 240 mL in 1 BOTTLE, PLASTIC (66689-201-08) | 03 Oct, 2006 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Purpose:
Purpose poison adsorbent
Product Elements:
Insta-char aqueous poison treatment adsorbent anhydrous citric acid glycerin propylene glycol water sucrose activated charcoal activated charcoal
Indications and Usage:
Uses for emergency use to adsorb swallowed poisons
Warnings:
Warnings do not use until after the patient has vomited, unless directed by a health professional in persons that are not fully conscious unless directed by a health professional, if turpentine, corrosives, such as alkalies (lye) and strong acids, or petroleum distillates, such as kerosene, gasoline, paint thinner, cleaning fluid or furniture polish, have been ingested if pregnant or breast-feeding, ask a health professional before use. keep out of reach of children.
Do Not Use:
Warnings do not use until after the patient has vomited, unless directed by a health professional in persons that are not fully conscious unless directed by a health professional, if turpentine, corrosives, such as alkalies (lye) and strong acids, or petroleum distillates, such as kerosene, gasoline, paint thinner, cleaning fluid or furniture polish, have been ingested if pregnant or breast-feeding, ask a health professional before use. keep out of reach of children.
Dosage and Administration:
Directions 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. age dose adult 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.
Package Label Principal Display Panel:
Insta-char aqueous 240 ml insta-char aqueous poison adsorbent 240 ml distributed by: vistapharm inc. largo, fl 33771 instacharaq2
Further Questions:
Questions? 888-655-1505