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  4. NDC Product Code: 22431-359 Relief Soothing Bath Treatment

NDC 22431-359 Relief Soothing Bath Treatment

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 22431-359?
  4. Relief Soothing Bath Treatment Uses
  5. Active Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
22431-359
Proprietary Name:
Relief Soothing Bath Treatment
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Blue Cross Laboratories, Inc.
Labeler Code:
22431
Product Label ID:
d8deb0ff-1d5f-41e3-919f-d6c4ef9810ce
Start Marketing Date: [9]
09-17-2010
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 22431-359?

The NDC code 22431-359 is assigned by the FDA to the product Relief Soothing Bath Treatment which is product labeled by Blue Cross Laboratories, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 22431-359-03 3 box in 1 box / 6 packet in 1 box (22431-359-02) / 42.5 g in 1 packet (22431-359-01). 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 Relief Soothing Bath Treatment?

When using this product do not get into eyesin some skin conditions, soaking too long may overdryto avoid slipping, use mat in tub or shower

Which are Relief Soothing Bath Treatment UNII Codes?

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

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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".