NDC 74530-054 Disney Minnie Mouse Antibacterial Hand Wipes

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:
74530-054
Proprietary Name:
Disney Minnie Mouse Antibacterial Hand Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Best Brand Consumers Products, Inc.
Labeler Code:
74530
Start Marketing Date: [9]
10-02-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 74530-054-01

Package Description: 25 SOLUTION in 1 BAG

NDC Code 74530-054-02

Package Description: 40 SOLUTION in 1 BAG

Product Details

What is NDC 74530-054?

The NDC code 74530-054 is assigned by the FDA to the product Disney Minnie Mouse Antibacterial Hand Wipes which is product labeled by Best Brand Consumers Products, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 74530-054-01 25 solution in 1 bag , 74530-054-02 40 solution in 1 bag . 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 Disney Minnie Mouse Antibacterial Hand Wipes?

Adults and children 3 years and over:Apply to hands Allow skin to dry without wipingFor children under 3 yearsAsk a doctor before use

Which are Disney Minnie Mouse Antibacterial Hand Wipes UNII Codes?

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

Which are Disney Minnie Mouse Antibacterial Hand 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:

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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".