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  4. NDC Product Code: 78580-010 Rolhei 75 Percent Ethanol Wet Wipe

NDC 78580-010 Rolhei 75 Percent Ethanol Wet Wipe

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 78580-010?
  4. Rolhei 75 Percent Ethanol Wet Wipe 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:
78580-010
Proprietary Name:
Rolhei 75 Percent Ethanol Wet Wipe
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Glory Co., Ltd.
Labeler Code:
78580
Product Label ID:
0479f4af-249e-446f-b84a-c8bd101db586
Start Marketing Date: [9]
06-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 78580-010-01

Package Description: 100 CLOTH in 1 PACKET

Product Details

What is NDC 78580-010?

The NDC code 78580-010 is assigned by the FDA to the product Rolhei 75 Percent Ethanol Wet Wipe which is product labeled by Glory Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 78580-010-01 100 cloth in 1 packet . 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 Rolhei 75 Percent Ethanol Wet Wipe?

■ Wet hands thoroughly with product and allow to dry without wiping■ Do not flush■ Children under 2 years ask a doctor before use

Which are Rolhei 75 Percent Ethanol Wet Wipe UNII Codes?

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

Which are Rolhei 75 Percent Ethanol Wet Wipe 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".