NDC 79887-112 Boosietizer Peach Scent

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:
79887-112
Proprietary Name:
Boosietizer Peach Scent
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Awsm Marcin Szakola
Labeler Code:
79887
Start Marketing Date: [9]
08-03-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
PEACH (C73407)

Product Packages

NDC Code 79887-112-23

Package Description: 200 mL in 1 BOTTLE

NDC Code 79887-112-53

Package Description: 500 mL in 1 BOTTLE

Product Details

What is NDC 79887-112?

The NDC code 79887-112 is assigned by the FDA to the product Boosietizer Peach Scent which is product labeled by Awsm Marcin Szakola. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 79887-112-23 200 ml in 1 bottle , 79887-112-53 500 ml 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 Boosietizer Peach Scent?

Place enough product on hands to cover all surfaces. Rub hands together until dry.Supervise children under 12 years of age when using this product to avoid swallowing.

Which are Boosietizer Peach Scent UNII Codes?

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

Which are Boosietizer Peach Scent 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".