NDC 22431-124 Epsom Salts Relief

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:
22431-124
Proprietary Name:
Epsom Salts Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Blue Cross Laboratories, Inc.
Labeler Code:
22431
Start Marketing Date: [9]
07-09-2010
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 22431-124-01

Package Description: 1810 g in 1 BAG

NDC Code 22431-124-02

Package Description: 454 g in 1 BAG

NDC Code 22431-124-03

Package Description: 454 g in 1 CARTON

NDC Code 22431-124-04

Package Description: 907 g in 1 BAG

Product Details

What is NDC 22431-124?

The NDC code 22431-124 is assigned by the FDA to the product Epsom Salts Relief which is product labeled by Blue Cross Laboratories, Inc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 22431-124-01 1810 g in 1 bag , 22431-124-02 454 g in 1 bag , 22431-124-03 454 g in 1 carton , 22431-124-04 907 g in 1 bag . 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 Epsom Salts Relief?

-For relief of occasional constipation (irregularity)-this product generally produces bowel movement in 1/2 to 6 hours

Which are Epsom Salts Relief UNII Codes?

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

  • MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T)
  • MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)

What is the NDC to RxNorm Crosswalk for Epsom Salts Relief?

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:

* 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".