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  4. NDC Product Code: 77110-600 Hand Sanitizing

NDC 77110-600 Hand Sanitizing

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 77110-600?
  4. Hand Sanitizing 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:
77110-600
Proprietary Name:
Hand Sanitizing
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Biominerales Pharma
Labeler Code:
77110
Product Label ID:
2ff3d532-1dee-4cfb-8852-20f654fb8b61
Start Marketing Date: [9]
09-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 77110-600-01

Package Description: 3785 mL in 1 CONTAINER

NDC Code 77110-600-02

Package Description: 946 mL in 1 CONTAINER

NDC Code 77110-600-03

Package Description: 473 mL in 1 CONTAINER

NDC Code 77110-600-04

Package Description: 236 mL in 1 CONTAINER

Product Details

What is NDC 77110-600?

The NDC code 77110-600 is assigned by the FDA to the product Hand Sanitizing which is product labeled by Biominerales Pharma. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 77110-600-01 3785 ml in 1 container , 77110-600-02 946 ml in 1 container , 77110-600-03 473 ml in 1 container , 77110-600-04 236 ml in 1 container . 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 Hand Sanitizing?

Rub thoroughly into hands for at least 30 seconds, allow to dry.Supervise children when they use this product.Adults and children 2 years and older:For occasional and personal domestic use.

Which are Hand Sanitizing UNII Codes?

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

Which are Hand Sanitizing 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 Hand Sanitizing?

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".