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  4. NDC Product Code: 50346-005 Pan Aromas Baby

NDC 50346-005 Pan Aromas Baby

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50346-005?
  4. Pan Aromas 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:
50346-005
Proprietary Name:
Pan Aromas Baby
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pan Aromas Llc
Labeler Code:
50346
Product Label ID:
cca5a149-01ed-41f8-9cb7-258b94ac94ab
Start Marketing Date: [9]
12-20-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 50346-005?

The NDC code 50346-005 is assigned by the FDA to the product Pan Aromas Baby which is product labeled by Pan Aromas Llc. The product's dosage form is . The product is distributed in 8 packages with assigned NDC codes 50346-005-16 100 ml in 1 bottle , 50346-005-17 192 ml in 1 bottle , 50346-005-18 200 ml in 1 bottle , 50346-005-19 296 ml in 1 bottle , 50346-005-20 355 ml in 1 bottle , 50346-005-21 414 ml in 1 bottle , 50346-005-22 474 ml in 1 bottle , 50346-005-23 590 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 Pan Aromas Baby?

UsesHelps moisturize delicate skin and helps prevent chafing.Use after shower or bath for superior moisturizing, helping skin stay soft and smooth.Also used as make-up remover from delicate skin.

Which are Pan Aromas Baby UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Pan Aromas 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".