NDC 68788-9801 Emetrol Cherry

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
68788-9801
Proprietary Name:
Emetrol Cherry
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Preferred Pharmaceuticals, Inc
Labeler Code:
68788
Start Marketing Date: [9]
04-23-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
RED (C48326 - RED)
Flavor(s):
CHERRY (C73375)

Product Packages

NDC Code 68788-9801-1

Package Description: 118 mL in 1 BOTTLE

Product Details

What is NDC 68788-9801?

The NDC code 68788-9801 is assigned by the FDA to the product Emetrol Cherry which is product labeled by Preferred Pharmaceuticals, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 68788-9801-1 118 ml in 1 bottle . 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 Emetrol Cherry?

For maximum effectiveness never dilute or drink fluids of any kind immediately before or after taking this productadults and children 12 years of age and over: one to two tablespoonschildren 2 to under 12: one or two teaspoonsrepeat dose every 15 minutes or until distress subsidesdo not take more than 5 doses in 1 hour without consulting a doctor

Which are Emetrol Cherry UNII Codes?

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

Which are Emetrol Cherry 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:

What is the NDC to RxNorm Crosswalk for Emetrol Cherry?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 318146 - dextrose 1.87 GM / fructose 1.87 GM / phosphoric acid 21.5 MG in 5 mL Oral Solution
  • RxCUI: 318146 - fructose 374 MG/ML / glucose 374 MG/ML / phosphoric acid 4.3 MG/ML Oral Solution
  • RxCUI: 318146 - dextrose 1.87 GM / fructose 1.87 GM / phosphoric acid 21.5 MG per 5 ML Oral Solution
  • RxCUI: 809602 - Emetrol 1.87 GM / 1.87 GM / 21.5 MG in 5 mL Oral Solution
  • RxCUI: 809602 - fructose 374 MG/ML / glucose 374 MG/ML / phosphoric acid 4.3 MG/ML Oral Solution [Emetrol]

* 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.

[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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".