NDC 23058-0150 Goop Hand Sanitizer Wipe

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:
23058-0150
Proprietary Name:
Goop Hand Sanitizer Wipe
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Critzas Industries, Inc.
Labeler Code:
23058
Start Marketing Date: [9]
09-24-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 23058-0150-1

Package Description: 1041 mL in 1 CANISTER

NDC Code 23058-0150-2

Package Description: 930 mL in 1 CANISTER

Product Details

What is NDC 23058-0150?

The NDC code 23058-0150 is assigned by the FDA to the product Goop Hand Sanitizer Wipe which is product labeled by Critzas Industries, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 23058-0150-1 1041 ml in 1 canister , 23058-0150-2 930 ml 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 Goop Hand Sanitizer Wipe?

Place enough product on 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 Goop Hand Sanitizer Wipe UNII Codes?

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

Which are Goop Hand Sanitizer Wipe 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 Goop Hand Sanitizer Wipe?

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".