NDC 76896-004 Antibacterial 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:
76896-004
Proprietary Name:
Antibacterial Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Zhejiang Binger Nonwoven Co., Ltd.
Labeler Code:
76896
Start Marketing Date: [9]
06-19-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 76896-004-01

Package Description: 10 POUCH in 1 BAG / 4.9 g in 1 POUCH

NDC Code 76896-004-02

Package Description: 20 POUCH in 1 BAG / 4.9 g in 1 POUCH

NDC Code 76896-004-03

Package Description: 100 POUCH in 1 BAG / 4.9 g in 1 POUCH

NDC Code 76896-004-04

Package Description: 50 POUCH in 1 BAG / 4.9 g in 1 POUCH

NDC Code 76896-004-05

Package Description: 60 POUCH in 1 BOTTLE / 4.9 g in 1 POUCH

NDC Code 76896-004-06

Package Description: 80 POUCH in 1 BOTTLE / 4.9 g in 1 POUCH

NDC Code 76896-004-07

Package Description: 100 POUCH in 1 BOTTLE / 4.9 g in 1 POUCH

NDC Code 76896-004-08

Package Description: 120 POUCH in 1 BOTTLE / 4.9 g in 1 POUCH

NDC Code 76896-004-09

Package Description: 1000 POUCH in 1 BOTTLE / 4.9 g in 1 POUCH

NDC Code 76896-004-10

Package Description: 80 POUCH in 1 BAG / 4.9 g in 1 POUCH

Product Details

What is NDC 76896-004?

The NDC code 76896-004 is assigned by the FDA to the product Antibacterial Wipes which is product labeled by Zhejiang Binger Nonwoven Co., Ltd.. The product's dosage form is . The product is distributed in 10 packages with assigned NDC codes 76896-004-01 10 pouch in 1 bag / 4.9 g in 1 pouch, 76896-004-02 20 pouch in 1 bag / 4.9 g in 1 pouch, 76896-004-03 100 pouch in 1 bag / 4.9 g in 1 pouch, 76896-004-04 50 pouch in 1 bag / 4.9 g in 1 pouch, 76896-004-05 60 pouch in 1 bottle / 4.9 g in 1 pouch, 76896-004-06 80 pouch in 1 bottle / 4.9 g in 1 pouch, 76896-004-07 100 pouch in 1 bottle / 4.9 g in 1 pouch, 76896-004-08 120 pouch in 1 bottle / 4.9 g in 1 pouch, 76896-004-09 1000 pouch in 1 bottle / 4.9 g in 1 pouch, 76896-004-10 80 pouch in 1 bag / 4.9 g in 1 pouch. 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 Antibacterial Wipes?

■I Wet hands thoroughly with product and allow to dry without wiping■I for children| under 6, use only under adult supervision ■not recommended for infants Other information 1 1 Keep containers tightly closed in a dry, cool and well-ventilated place. ■Recommended storage temperature: 32°F to 104°F (0°C to 40°C)

Which are Antibacterial Wipes UNII Codes?

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

Which are Antibacterial 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 Antibacterial 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".