NDC 78985-002 Hand Sanitizing And Moisturizing 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:
78985-002
Proprietary Name:
Hand Sanitizing And Moisturizing Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Generic Specialties, Inc.
Labeler Code:
78985
Start Marketing Date: [9]
09-21-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 78985-002-09

Package Description: 30 SWAB in 1 POUCH

NDC Code 78985-002-11

Package Description: 60 SWAB in 1 POUCH

NDC Code 78985-002-18

Package Description: 180 SWAB in 1 CANISTER

NDC Code 78985-002-19

Package Description: 20 SWAB in 1 POUCH

NDC Code 78985-002-20

Package Description: 160 SWAB in 1 CANISTER

Product Details

What is NDC 78985-002?

The NDC code 78985-002 is assigned by the FDA to the product Hand Sanitizing And Moisturizing Wipes which is product labeled by Generic Specialties, Inc.. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 78985-002-09 30 swab in 1 pouch , 78985-002-11 60 swab in 1 pouch , 78985-002-18 180 swab in 1 canister , 78985-002-19 20 swab in 1 pouch , 78985-002-20 160 swab in 1 canister . 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 Hand Sanitizing And Moisturizing Wipes?

Wipe hands thoroughly with a towelette. Allow to dry. Discard after a single-use. For External use only.

Which are Hand Sanitizing And Moisturizing Wipes UNII Codes?

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

Which are Hand Sanitizing And Moisturizing 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:

* 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".