NDC 81886-101 Hand Sanitizer Alcohol 75%

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:
81886-101
Proprietary Name:
Hand Sanitizer Alcohol 75%
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
81886
Start Marketing Date: [9]
05-12-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 81886-101?

The NDC code 81886-101 is assigned by the FDA to the product Hand Sanitizer Alcohol 75% which is product labeled by Frog Prince (fujian) Baby & Child Care Products Co., Ltd.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 81886-101-11 30 ml in 1 packet , 81886-101-12 27 ml in 1 packet . 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 Alcohol 75%?

PLACE ENOUGH PRODUCT IN YOUR HANDS TO COVER ALL SURFACES. RUB HANDS TOGETHER UNTIL DRY.SUPERVISE CHILDREN UNDER 6 YEARS OF AGE WHEN USING THIS PRODUCT TO AVOID SWALLOWING.

Which are Hand Sanitizer Alcohol 75% UNII Codes?

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

Which are Hand Sanitizer Alcohol 75% 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 Hand Sanitizer Alcohol 75%?

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:

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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".