NDC 64616-047 Bye Bye Diaper Rash

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:
64616-047
Proprietary Name:
Bye Bye Diaper Rash
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Vitality Works, Inc.
Labeler Code:
64616
Start Marketing Date: [9]
10-26-2005
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 64616-047-02

Package Description: 1 BOTTLE, SPRAY in 1 CARTON / 59 mL in 1 BOTTLE, SPRAY (64616-047-01)

Product Details

What is NDC 64616-047?

The NDC code 64616-047 is assigned by the FDA to the product Bye Bye Diaper Rash which is product labeled by Vitality Works, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64616-047-02 1 bottle, spray in 1 carton / 59 ml in 1 bottle, spray (64616-047-01). 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.

Which are Bye Bye Diaper Rash UNII Codes?

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

Which are Bye Bye Diaper Rash 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".