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  4. NDC Product Code: 60681-6001 Pleo Alkala Antacid

NDC 60681-6001 Pleo Alkala Antacid

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 60681-6001?
  4. Pleo Alkala Antacid Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
60681-6001
Proprietary Name:
Pleo Alkala Antacid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sanum Kehlbeck Gmbh & Co. Kg
Labeler Code:
60681
Product Label ID:
7dca3271-4810-45d0-8b02-0bb0941bcc6f
Start Marketing Date: [9]
12-19-1996
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 60681-6001?

The NDC code 60681-6001 is assigned by the FDA to the product Pleo Alkala Antacid which is product labeled by Sanum Kehlbeck Gmbh & Co. Kg. The product's dosage form is . The product is distributed in a single package with assigned NDC code 60681-6001-1 1 bottle, plastic in 1 carton / 150 g 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 Pleo Alkala Antacid?

Use enclosed spoon. Take one spoonful in the morning with a glass of water. If needed, take a second spoonful in the evening, or as directed by a doctor.Do not take more than 2 spoonfuls in a 24-hour period. If you are over 60 years old, do not take more than 1 spoonful. Not for children under 12 years.Do not take maximum dose for more than 2 weeks.

Which are Pleo Alkala Antacid UNII Codes?

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

Which are Pleo Alkala Antacid 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 Pleo Alkala Antacid?

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: 1251780 - potassium bicarbonate 7.8 % / sodium bicarbonate 78 % / sodium citrate 1.6 % Powder for Oral Solution
  • RxCUI: 1251780 - potassium bicarbonate 11700 MG / sodium bicarbonate 117000 MG / sodium citrate 2400 MG Powder for Oral Solution
  • RxCUI: 1251780 - K+ bicarbonate 11700 MG / NaHCO3 117000 MG / sodium citrate 2400 MG Powder for Oral Solution
  • RxCUI: 1251780 - Pot bicarbonate 11700 MG / NaHCO3 117000 MG / sodium citrate 2400 MG Powder for Oral Solution
  • RxCUI: 1251782 - Pleo Alkala 7.8 % / 78 % / 1.6 % Powder for Oral Solution

* 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".