NDC 71766-002 Hand Sanitizer 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:
71766-002
Proprietary Name:
Hand Sanitizer Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hangzhou Linkeweier Daily Chemicals Co., Ltd.
Labeler Code:
71766
Start Marketing Date: [9]
02-20-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71766-002-01

Package Description: 60 BOTTLE in 1 CARTON / 30 GEL in 1 BOTTLE

Product Details

What is NDC 71766-002?

The NDC code 71766-002 is assigned by the FDA to the product Hand Sanitizer Wipes which is product labeled by Hangzhou Linkeweier Daily Chemicals Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71766-002-01 60 bottle in 1 carton / 30 gel in 1 bottle. 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 Sanitizer Wipes?

Slowly peel back label and use one wipe. Reseal, keep closed to prevent evaporation. Thoroughly wipe hands, allow to dry out rinsing. Discard after single useOther information Do not flush down toilet. Keep away from sunlight. Store at room temperature 20°-25°Celsius (68°-77° Fahrenheit) May discolor certain fabrics

Which are Hand Sanitizer Wipes UNII Codes?

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

Which are Hand Sanitizer 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".