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  4. NDC Product Code: 51346-435 Vitamin B5

NDC 51346-435 Vitamin B5

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51346-435?
  4. Vitamin B5 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:
51346-435
Proprietary Name:
Vitamin B5
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nature Republic Co., Ltd.
Labeler Code:
51346
Product Label ID:
ecc66127-66f7-45a5-b02f-b4f3b4cfe768
Start Marketing Date: [9]
12-01-2016
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 51346-435?

The NDC code 51346-435 is assigned by the FDA to the product Vitamin B5 which is product labeled by Nature Republic Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51346-435-02 1 bottle, plastic in 1 carton / 150 ml in 1 bottle, plastic (51346-435-01). 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.

What are the uses for Vitamin B5?

Indications & Usage: The vitamin B5 emulsion helps sensitive skin feel moisturized and radiant.

Which are Vitamin B5 UNII Codes?

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

Which are Vitamin B5 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 Vitamin B5?

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".