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  4. NDC Product Code: 78885-100 E D Alcohol Wipes 100

NDC 78885-100 E D Alcohol Wipes 100

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 78885-100?
  4. E D Alcohol Wipes 100 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:
78885-100
Proprietary Name:
E D Alcohol Wipes 100
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ensobretados Y Derivados S.a. De C.v.
Labeler Code:
78885
Product Label ID:
aaab23af-f048-fdb2-e053-2995a90ae61c
Start Marketing Date: [9]
07-15-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 78885-100-00

Package Description: 100 PACKET in 1 BOX / 1 mL in 1 PACKET

Product Details

What is NDC 78885-100?

The NDC code 78885-100 is assigned by the FDA to the product E D Alcohol Wipes 100 which is product labeled by Ensobretados Y Derivados S.a. De C.v.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 78885-100-00 100 packet in 1 box / 1 ml 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 E D Alcohol Wipes 100?

■ Wet hands thoroughly. Allow to dry without wiping.■ Supervise children under 6 years of age when using this product to avoid swallowing.

Which are E D Alcohol Wipes 100 UNII Codes?

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

Which are E D Alcohol Wipes 100 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".