NDC 74763-005 Alcohol 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:
74763-005
Proprietary Name:
Alcohol Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Zhejiang Gafle Auto Chemical Co.,ltd
Labeler Code:
74763
Start Marketing Date: [9]
04-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 74763-005-01

Package Description: 100 CLOTH in 1 BAG

NDC Code 74763-005-02

Package Description: 120 CLOTH in 1 BAG

NDC Code 74763-005-03

Package Description: 160 CLOTH in 1 BAG

Product Details

What is NDC 74763-005?

The NDC code 74763-005 is assigned by the FDA to the product Alcohol Wipes which is product labeled by Zhejiang Gafle Auto Chemical Co.,ltd. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 74763-005-01 100 cloth in 1 bag , 74763-005-02 120 cloth in 1 bag , 74763-005-03 160 cloth 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 Alcohol Wipes?

1. Lift the tab on the top of the lid to open. 2. Open moisture seal film package before use. 3. Pull out first wipe through the dispensing center of the canister. Next sheets pops up automatically 4. Close the lid to retain moisture. 5. Wipe dean with this product. Let air dry

Which are Alcohol Wipes UNII Codes?

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

Which are 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:

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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".