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  4. NDC Product Code: 37205-178 Soothing Bath Treatment

NDC 37205-178 Soothing Bath Treatment

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 37205-178?
  4. 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:
37205-178
Proprietary Name:
Soothing Bath Treatment
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cardinal Health
Labeler Code:
37205
Product Label ID:
a9742bef-3749-4d3f-b479-1ac88fce9a96
Start Marketing Date: [9]
07-21-2005
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 37205-178?

The NDC code 37205-178 is assigned by the FDA to the product Soothing Bath Treatment which is product labeled by Cardinal Health. The product's dosage form is . The product is distributed in a single package with assigned NDC code 37205-178-51 8 packet in 1 carton / 42.5 g in 1 packet. 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 Soothing Bath Treatment?

Turn warm water faucet on to full force.Slowly sprinkle 1 packet of colloidal oatmeal directly under the faucet into the tub or container.Stir any colloidal oatmeal that may have settled to the bottom.Soak affected area for 15-30 minutes as needed or as directed by a doctor.Pat dry (do not rub) to keep a thin layer on the skin.

Which are Soothing Bath Treatment UNII Codes?

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

* Please review the disclaimer below.

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".