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  4. NDC Product Code: 49738-395 Epsom Salt

NDC 49738-395 Epsom Salt

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 49738-395?
  4. Epsom Salt Uses
  5. Active Ingredients UNII Codes
  6. 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:
49738-395
Proprietary Name:
Epsom Salt
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Smart Sense (kmart)
Labeler Code:
49738
Product Label ID:
708ed5a1-7808-490d-9b1f-fa36aa709a57
Start Marketing Date: [9]
07-31-2017
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 49738-395?

The NDC code 49738-395 is assigned by the FDA to the product Epsom Salt which is product labeled by Smart Sense (kmart). The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 49738-395-01 454 g in 1 pouch , 49738-395-04 1814 g in 1 pouch , 49738-395-06 2720 g in 1 pouch . 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 Salt?

Do not exceed more than 2 doses per day; if necessary repeat dosage in 4 hoursagedose adults and children 12  years and older2-4 level teaspoons dissolved in a full glass (8oz) of water  children 6 to 11 years1-2 level teaspoons dissolved in a full glass (8oz) of waterNot recommended for children under 6 years of age.

Which are Epsom Salt UNII Codes?

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

  • MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
  • MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)

What is the NDC to RxNorm Crosswalk for Epsom Salt?

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:

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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".