NDC 51345-099 Epsom Salt Soaking Solution

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:
51345-099
Proprietary Name:
Epsom Salt Soaking Solution
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Advanced Beauty Systems, Inc.
Labeler Code:
51345
Start Marketing Date: [9]
06-13-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51345-099-01

Package Description: 2.72 kg in 1 BAG

Product Details

What is NDC 51345-099?

The NDC code 51345-099 is assigned by the FDA to the product Epsom Salt Soaking Solution which is product labeled by Advanced Beauty Systems, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51345-099-01 2.72 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 Epsom Salt Soaking Solution?

When using this product, do not use more than directed.Stop use and consult a doctor if:As a soaking solution- you experience redness, irritation, swelling , or infectionAs a laxative- you have no bowel movements within six hours or experience rectal bleeding-these could be signs of a serious condition- you need a laxative for more than a week

Which are Epsom Salt Soaking Solution UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Epsom Salt Soaking Solution?

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".