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  4. NDC Product Code: 15071-804 Rash Relief Antifungal

NDC 15071-804 Rash Relief Antifungal

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 15071-804?
  4. Rash Relief Antifungal Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
15071-804
Proprietary Name:
Rash Relief Antifungal
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Touchless Care Concepts Llc
Labeler Code:
15071
Product Label ID:
4114c685-acd1-4c65-842b-1cb7840852dc
Start Marketing Date: [9]
06-14-2006
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 15071-804-11

Package Description: 56 g in 1 BOTTLE

Product Details

What is NDC 15071-804?

The NDC code 15071-804 is assigned by the FDA to the product Rash Relief Antifungal 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 15071-804-11 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 Antifungal?

- Clean the affected area and dry thoroughly.  - Shake bottle well before use.- Spray 4-6 inches from skin twice daily (morning and night) or as directed by a physician.  No rub-in is required.

Which are Rash Relief Antifungal UNII Codes?

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

Which are Rash Relief Antifungal 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:

What is the NDC to RxNorm Crosswalk for Rash Relief Antifungal?

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:
  • RxCUI: 1000009 - miconazole nitrate 2 % / dimethicone 10 % / zinc oxide 10 % Topical Spray
  • RxCUI: 1000009 - dimethicone 100 MG/ML / miconazole nitrate 20 MG/ML / zinc oxide 100 MG/ML Topical Spray
  • RxCUI: 1000009 - dimethicone 10 % / miconazole nitrate 2 % / zinc oxide 10 % Topical Spray
  • RxCUI: 1000009 - dimethicone 100 MG/ML / Miconazole Nitrate 20 MG/ML / ZNO 100 MG/ML Topical Spray
  • RxCUI: 1089121 - RASH RELIEF Antifungal 2 % / 10 % / 10 % Topical Spray

* 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".