NDC 71544-0004 Beklyn Absolute Purifying Hand Gel

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
71544-0004
Proprietary Name:
Beklyn Absolute Purifying Hand Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
My Corp.,ltd
Labeler Code:
71544
Start Marketing Date: [9]
07-15-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71544-0004-1

Package Description: 300 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 71544-0004?

The NDC code 71544-0004 is assigned by the FDA to the product Beklyn Absolute Purifying Hand Gel which is product labeled by My Corp.,ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71544-0004-1 300 ml in 1 bottle, pump . 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 Beklyn Absolute Purifying Hand Gel?

Squeeze enough product in your palm to cover hands and rub hands together until dry.For children under 6 years use adult supervisionNot recommended for infants

Which are Beklyn Absolute Purifying Hand Gel UNII Codes?

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

Which are Beklyn Absolute Purifying Hand Gel 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".