NDC 78936-005 Sanitizing 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:
78936-005
Proprietary Name:
Sanitizing Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hangzhou Caring Cleaning Commodity Co.,ltd
Labeler Code:
78936
Start Marketing Date: [9]
07-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 78936-005-01

Package Description: 20 POUCH in 1 BAG / 1 mg in 1 POUCH

NDC Code 78936-005-02

Package Description: 30 PACKAGE in 1 BOX / 1 POUCH in 1 PACKAGE / 1 mg in 1 POUCH

NDC Code 78936-005-03

Package Description: 100 PACKAGE in 1 BOX / 1 POUCH in 1 PACKAGE / 1 mg in 1 POUCH

Product Details

What is NDC 78936-005?

The NDC code 78936-005 is assigned by the FDA to the product Sanitizing Wipes which is product labeled by Hangzhou Caring Cleaning Commodity Co.,ltd. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 78936-005-01 20 pouch in 1 bag / 1 mg in 1 pouch, 78936-005-02 30 package in 1 box / 1 pouch in 1 package / 1 mg in 1 pouch, 78936-005-03 100 package in 1 box / 1 pouch in 1 package / 1 mg 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 Sanitizing Wipes?

Storage.Store at room temperature.Dispensing.Tear open packet.Unfold towelette.Use.Apply wipe thoroughly to hands as desired.Allow to dry without wiping.Disposal.Dispose of used wipes in trash receptacle after use.Do not flush.

Which are Sanitizing Wipes UNII Codes?

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

Which are Sanitizing 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".