NDC 52000-006 Universal Baby Fresh Scent Petroleum

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:
52000-006
Proprietary Name:
Universal Baby Fresh Scent Petroleum
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
52000
Start Marketing Date: [9]
02-06-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 52000-006?

The NDC code 52000-006 is assigned by the FDA to the product Universal Baby Fresh Scent Petroleum which is product labeled by Universal Distribution Center Llc. The product's dosage form is . The product is distributed in 10 packages with assigned NDC codes 52000-006-19 226 g in 1 jar , 52000-006-20 45 g in 1 jar , 52000-006-21 100 g in 1 jar , 52000-006-22 113 g in 1 jar , 52000-006-23 170 g in 1 jar , 52000-006-24 198 g in 1 jar , 52000-006-25 283 g in 1 jar , 52000-006-26 368 g in 1 jar , 52000-006-27 450 g in 1 jar , 52000-006-28 500 g in 1 jar . 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 Universal Baby Fresh Scent Petroleum?

UsesFor the temporary protection of minor cuts, scrapes, burns and sunburn.Helps to temporarily protect chafed, chapped, cracked or windburned skin and lips.

Which are Universal Baby Fresh Scent Petroleum UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Universal Baby Fresh Scent Petroleum?

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".