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NDC 37808-082 Orchid By H E B Cactus Flower And Mango Antibacterial Gentle Foaming Hand

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 37808-082?
  4. Orchid By H E B Cactus Flower And Mango Antibacterial Gentle Foaming Hand 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:
37808-082
Proprietary Name:
Orchid By H E B Cactus Flower And Mango Antibacterial Gentle Foaming Hand
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
H E B
Labeler Code:
37808
Product Label ID:
15ef5e98-93c4-4a6c-ab9b-2352c69f89a6
Start Marketing Date: [9]
07-31-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 37808-082-08

Package Description: 236 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 37808-082?

The NDC code 37808-082 is assigned by the FDA to the product Orchid By H E B Cactus Flower And Mango Antibacterial Gentle Foaming Hand which is product labeled by H E B. The product's dosage form is . The product is distributed in a single package with assigned NDC code 37808-082-08 236 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 Orchid By H E B Cactus Flower And Mango Antibacterial Gentle Foaming Hand?

APPLY TO DRY HANDS, LATHER AND RINSE THOROUGHLY

Which are Orchid By H E B Cactus Flower And Mango Antibacterial Gentle Foaming Hand UNII Codes?

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

Which are Orchid By H E B Cactus Flower And Mango Antibacterial Gentle Foaming Hand 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".