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  4. NDC Product Code: 15071-652 Rash Relief Silver

NDC 15071-652 Rash Relief Silver

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 15071-652?
  4. Rash Relief Silver Uses
  5. Active Ingredients UNII Codes
  6. Inactive 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:
15071-652
Proprietary Name:
Rash Relief Silver
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Touchless Care Concepts Llc
Labeler Code:
15071
Product Label ID:
4de4d6a4-db9d-4eed-badc-a365af191e84
Start Marketing Date: [9]
11-01-2008
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 15071-652?

The NDC code 15071-652 is assigned by the FDA to the product Rash Relief Silver which is product labeled by Touchless Care Concepts Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 15071-652-11 56 g in 1 bottle . 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 Rash Relief Silver?

- Cleanse the skin area thoroughly.  - Shake bottle well before use.- Spray 4-6 inches from skin using firm/quick trigger motion. No rub-in is required.  Coating slowly dries over time.- Reapply 1-3 times per day or as directed by health professional.

Which are Rash Relief Silver UNII Codes?

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

Which are Rash Relief Silver Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive 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".