NDC 79014-001 Defender 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:
79014-001
Proprietary Name:
Defender Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wenzhou Bofeng Packaging Co., Ltd.
Labeler Code:
79014
Start Marketing Date: [9]
06-15-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 79014-001-01

Package Description: 1 PATCH in 1 BAG / 3.5 g in 1 PATCH

NDC Code 79014-001-02

Package Description: 10 PATCH in 1 BAG / 3.5 g in 1 PATCH

NDC Code 79014-001-03

Package Description: 15 PATCH in 1 BAG / 3.5 g in 1 PATCH

NDC Code 79014-001-04

Package Description: 20 PATCH in 1 BAG / 3.5 g in 1 PATCH

Product Details

What is NDC 79014-001?

The NDC code 79014-001 is assigned by the FDA to the product Defender Wipes which is product labeled by Wenzhou Bofeng Packaging Co., Ltd.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 79014-001-01 1 patch in 1 bag / 3.5 g in 1 patch, 79014-001-02 10 patch in 1 bag / 3.5 g in 1 patch, 79014-001-03 15 patch in 1 bag / 3.5 g in 1 patch, 79014-001-04 20 patch in 1 bag / 3.5 g in 1 patch. 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 Defender Wipes?

Tear V notch located on top of the plastic bag.Pull out the first wipe approximately 6 to 8 inches from the center of the roll.Place entire bag inside of center pull dispenser.Close the lid of the dispenser. Wipe dispensing tension may be adjusted on the top of the dispenser. Dispenser must be mounted with wipes dispensing up.Apply topically to the skin to help prevent cross contamination.Recommended for repeated use.Dries in seconds.

Which are Defender Wipes UNII Codes?

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

Which are Defender 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 Defender 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:

* Please review the disclaimer below.

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".