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  4. NDC Product Code: 77720-015 Hand Alcohol Wipes

NDC 77720-015 Hand Alcohol Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 77720-015?
  4. Hand Alcohol Wipes 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:
77720-015
Proprietary Name:
Hand Alcohol Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Skaffles Group Limited Liability Company
Labeler Code:
77720
Product Label ID:
b7b9e51c-c314-1015-e053-2a95a90abc3d
Start Marketing Date: [9]
12-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 77720-015-01

Package Description: 10 NOT APPLICABLE in 1 POUCH / 40.5 mL in 1 NOT APPLICABLE

NDC Code 77720-015-02

Package Description: 15 NOT APPLICABLE in 1 POUCH / 60.7 mL in 1 NOT APPLICABLE

NDC Code 77720-015-03

Package Description: 20 NOT APPLICABLE in 1 POUCH / 81 mL in 1 NOT APPLICABLE

NDC Code 77720-015-04

Package Description: 25 NOT APPLICABLE in 1 POUCH / 101 mL in 1 NOT APPLICABLE

NDC Code 77720-015-05

Package Description: 30 POUCH in 1 POUCH / 121 mL in 1 POUCH

NDC Code 77720-015-06

Package Description: 50 NOT APPLICABLE in 1 BAG / 202 mL in 1 NOT APPLICABLE

NDC Code 77720-015-07

Package Description: 75 NOT APPLICABLE in 1 CANISTER / 303 mL in 1 NOT APPLICABLE

NDC Code 77720-015-08

Package Description: 100 NOT APPLICABLE in 1 POUCH / 405 mL in 1 NOT APPLICABLE

NDC Code 77720-015-09

Package Description: 1 POUCH in 1 POUCH / 2.56 mL in 1 POUCH

NDC Code 77720-015-10

Package Description: 50 NOT APPLICABLE in 1 CANISTER / 202 mL in 1 NOT APPLICABLE

Product Details

What is NDC 77720-015?

The NDC code 77720-015 is assigned by the FDA to the product Hand Alcohol Wipes which is product labeled by Skaffles Group Limited Liability Company. The product's dosage form is . The product is distributed in 10 packages with assigned NDC codes 77720-015-01 10 not applicable in 1 pouch / 40.5 ml in 1 not applicable, 77720-015-02 15 not applicable in 1 pouch / 60.7 ml in 1 not applicable, 77720-015-03 20 not applicable in 1 pouch / 81 ml in 1 not applicable, 77720-015-04 25 not applicable in 1 pouch / 101 ml in 1 not applicable, 77720-015-05 30 pouch in 1 pouch / 121 ml in 1 pouch, 77720-015-06 50 not applicable in 1 bag / 202 ml in 1 not applicable, 77720-015-07 75 not applicable in 1 canister / 303 ml in 1 not applicable, 77720-015-08 100 not applicable in 1 pouch / 405 ml in 1 not applicable, 77720-015-09 1 pouch in 1 pouch / 2.56 ml in 1 pouch, 77720-015-10 50 not applicable in 1 canister / 202 ml in 1 not applicable. 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 Alcohol Wipes?

Directions● Adults and children 2 yrs and over, apply to hands and allow skin to dry without wiping. ●Children under 2, ask doctor before use.

Which are Hand Alcohol Wipes UNII Codes?

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

Which are Hand Alcohol Wipes 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 Alcohol Wipes?

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".