NDC 78451-001 Alcohol Moist 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:
78451-001
Proprietary Name:
Alcohol Moist Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Liaocheng Yadong Weiye Daily Necessities Co., Ltd
Labeler Code:
78451
Start Marketing Date: [9]
06-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Product Packages

NDC Code 78451-001-01

Package Description: 10 g in 1 PACKAGE

NDC Code 78451-001-02

Package Description: 30 g in 1 PACKAGE

NDC Code 78451-001-03

Package Description: 60 g in 1 PACKAGE

NDC Code 78451-001-04

Package Description: 80 g in 1 PACKAGE

Product Details

What is NDC 78451-001?

The NDC code 78451-001 is assigned by the FDA to the product Alcohol Moist Wipes which is product labeled by Liaocheng Yadong Weiye Daily Necessities Co., Ltd. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 78451-001-01 10 g in 1 package , 78451-001-02 30 g in 1 package , 78451-001-03 60 g in 1 package , 78451-001-04 80 g in 1 package . 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 Moist Wipes?

Foradults and children of 2 years and over.children under 2 years ask a doctor before useallow to dry without wiping.Directions Peel back flap on front to pull out a towelette. Unfold and wipe hands thoroughly. Reseal the flap. No need to rinse.

Which are Alcohol Moist Wipes UNII Codes?

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

Which are Alcohol Moist 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".