NDC 51619-600 Pepsom Flying P Epsom Salt

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:
51619-600
Proprietary Name:
Pepsom Flying P Epsom Salt
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
51619
Start Marketing Date: [9]
11-09-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 51619-600?

The NDC code 51619-600 is assigned by the FDA to the product Pepsom Flying P Epsom Salt which is product labeled by The Pepsom Group, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51619-600-84 1.81 kg 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 Pepsom Flying P Epsom Salt?

Soaking Solution:Bath - Dissolve 2 cups into a tub of hot water and soak for 15-30 minutesFoot or Wrist Soak - Dissolve 2 cups into a foot bath half-full of water, soaking the injured area for 20-30 minutes. Repeat 2-3 times per day until relief is obtainedLaxative:Children 6-12 years.........................Dissolve 1-2 level teaspoons(5mg-10mg) into a full cup of water (8oz)Adults and Children over 12.........Dissolve 2-4 level teaspoons(10mg-20mg) into a full cup of water (8oz)

Which are Pepsom Flying P 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 Pepsom Flying P 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".