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NDC 37808-168 Hill Country Essentials Antibacterial Foaming

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 37808-168?
  4. Hill Country Essentials Antibacterial Foaming Uses
  5. Active Ingredients UNII Codes
  6. 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:
37808-168
Proprietary Name:
Hill Country Essentials Antibacterial Foaming
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Heb
Labeler Code:
37808
Product Label ID:
1e05513c-b1db-45bb-bc9c-9f0fab40a525
Start Marketing Date: [9]
07-22-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 37808-168-08

Package Description: 222 mL in 1 BOTTLE, PLASTIC

NDC Code 37808-168-32

Package Description: 946 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 37808-168?

The NDC code 37808-168 is assigned by the FDA to the product Hill Country Essentials Antibacterial Foaming which is product labeled by Heb. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 37808-168-08 222 ml in 1 bottle, plastic , 37808-168-32 946 ml in 1 bottle, plastic . 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 Hill Country Essentials Antibacterial Foaming?

Apply onto dry hands, work into rich foamy lather, rinse and dry thoroughly

Which are Hill Country Essentials Antibacterial Foaming UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Hill Country Essentials Antibacterial Foaming?

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".