NDC 69017-100 Jouer Hand 2 Hand Hand 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:
69017-100
Proprietary Name:
Jouer Hand 2 Hand Hand Sanitizing Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jouer Cosmetics, Llc
Labeler Code:
69017
Start Marketing Date: [9]
06-23-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69017-100-01

Package Description: 25 PATCH in 1 PACKET / 100 L in 1 PATCH

Product Details

What is NDC 69017-100?

The NDC code 69017-100 is assigned by the FDA to the product Jouer Hand 2 Hand Hand Sanitizing Wipes which is product labeled by Jouer Cosmetics, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69017-100-01 25 patch in 1 packet / 100 l 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 Jouer Hand 2 Hand Hand Sanitizing Wipes?

Teapr open, unfold, and apply onto handsAllow to dry without wipingChildren under 6 years og age should be supervised when using this product

Which are Jouer Hand 2 Hand Hand Sanitizing Wipes UNII Codes?

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

Which are Jouer Hand 2 Hand Hand 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".