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NDC 37205-602 Epsom Salt

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 37205-602?
  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:
37205-602
Proprietary Name:
Epsom Salt
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cardinal Health
Labeler Code:
37205
Product Label ID:
88cad63f-8eb0-41b8-8d33-6b285a606c65
Start Marketing Date: [9]
03-26-2012
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 37205-602?

The NDC code 37205-602 is assigned by the FDA to the product Epsom Salt which is product labeled by Cardinal Health. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 37205-602-07 1814 g in 1 pouch , 37205-602-43 454 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 recommended daily dosagedrink a full glass (8 ounces) of liquid with each dosemay be taken as a single daily dose or in divided dosesdissolve the dose in 8 ounces of water. Lemon juice may be added to improve the taste.adults and children 12 years and over - 2 to 6 level teaspoons (10 to 30 grams) dailychildren 6 to under 12 years - 1 to 2 level teaspoons (5 to 10 grams) dailychildren under 6 years - consult a doctor

Which are Epsom Salt 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 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".