NDC 58737-151 Hand Sanitizer Frozen 6 Pack Frozen 6pack

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:
58737-151
Proprietary Name:
Hand Sanitizer Frozen 6 Pack Frozen 6pack
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
58737
Start Marketing Date: [9]
06-03-2016
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
VANILLA (C73421)
WATERMELON (C73423)
APPLE (C73362)
BLUEBERRY (C73367)
GRAPE (C73391)
STRAWBERRY (C73417)

Code Structure Chart

Product Details

What is NDC 58737-151?

The NDC code 58737-151 is assigned by the FDA to the product Hand Sanitizer Frozen 6 Pack Frozen 6pack which is product labeled by Townley, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 58737-151-01 59 g 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 Frozen 6 Pack Frozen 6pack?

Frozen 6 packCotton Candy Scentend Hand SanitizerCherry Scentend Hand SanitizerGrape Scentend Hand SanitizerBubble Gum Scentend Hand SanitizerLemon Scentend Hand SanitizerWatermelon Scentend Hand Sanitizer2 FL OZ (59mL)

Which are Hand Sanitizer Frozen 6 Pack Frozen 6pack UNII Codes?

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

Which are Hand Sanitizer Frozen 6 Pack Frozen 6pack 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".