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  4. NDC Product Code: 70359-4101 Buttiezzz Daily

NDC 70359-4101 Buttiezzz Daily

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70359-4101?
  4. Buttiezzz Daily Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
70359-4101
Proprietary Name:
Buttiezzz Daily
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Fortunique B.v.
Labeler Code:
70359
Product Label ID:
29b8e3ae-3006-3a96-e054-00144ff8d46c
Start Marketing Date: [9]
01-19-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 70359-4101?

The NDC code 70359-4101 is assigned by the FDA to the product Buttiezzz Daily which is product labeled by Fortunique B.v.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70359-4101-1 1 bottle, spray in 1 carton / 50 g in 1 bottle, spray. 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 Buttiezzz Daily?

Change wet or soiled diapers promptlyShake well before useMake sure the skin is clean and dry before use.Use a sweeping movement to spray-on the cream in a thin and uniform layer on the buttocksAllow to dryUse a spraying distance approximately 2 to 3 inchesApply Buttiezzz Daily liberally as often as necessary or at every diaper change

Which are Buttiezzz Daily UNII Codes?

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

Which are Buttiezzz Daily 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 Buttiezzz Daily?

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".