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  4. NDC Product Code: 69174-126 Tenzer Baby

NDC 69174-126 Tenzer Baby

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69174-126?
  4. Tenzer Baby Uses
  5. Active Ingredients UNII Codes
  6. 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:
69174-126
Proprietary Name:
Tenzer Baby
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Collection 2000 Cosmetics,inc.
Labeler Code:
69174
Product Label ID:
2b177667-ad01-4575-9ca2-7adb2b75b66a
Start Marketing Date: [9]
05-30-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 69174-126?

The NDC code 69174-126 is assigned by the FDA to the product Tenzer Baby which is product labeled by Collection 2000 Cosmetics,inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 69174-126-10 284 g in 1 container , 69174-126-13 368 g in 1 container . 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 Tenzer Baby?

Apply as needed

Which are Tenzer Baby UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Tenzer Baby?

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".