1. Home
  2. Labeler Index
  3. Mi Medical Supply
  4. NDC Product Code: 77508-101 The Upper Hand

NDC 77508-101 The Upper Hand

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 77508-101?
  4. The Upper Hand 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:
77508-101
Proprietary Name:
The Upper Hand
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mi Medical Supply
Labeler Code:
77508
Product Label ID:
a7326f3a-eb6a-146e-e053-2995a90a04d7
Start Marketing Date: [9]
06-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 77508-101?

The NDC code 77508-101 is assigned by the FDA to the product The Upper Hand which is product labeled by Mi Medical Supply. The product's dosage form is . The product is distributed in 7 packages with assigned NDC codes 77508-101-02 59.15 ml in 1 bottle , 77508-101-04 118.2 ml in 1 bottle , 77508-101-08 236.5 ml in 1 bottle, pump , 77508-101-16 473.17 ml in 1 bottle, pump , 77508-101-28 3785.41 ml in 1 bottle , 77508-101-32 946.35 ml in 1 bottle, pump , 77508-101-64 1892.71 ml 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 The Upper Hand?

Hand Sanitizer to help reduce bacteria on the skin that could cause disease.Recommended for Repeated use

Which are The Upper Hand UNII Codes?

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

Which are The Upper 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:

What is the NDC to RxNorm Crosswalk for The Upper Hand?

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:

* 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".