NDC 52069-100 Sofskin 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:
52069-100
Proprietary Name:
Sofskin Petroleum
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nova Petroleum & Chemicals Corporation
Labeler Code:
52069
Start Marketing Date: [9]
03-10-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 52069-100-08

Package Description: 110 g in 1 JAR

Product Details

What is NDC 52069-100?

The NDC code 52069-100 is assigned by the FDA to the product Sofskin Petroleum which is product labeled by Nova Petroleum & Chemicals Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52069-100-08 110 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 Sofskin Petroleum?

Apply product liberally, as often as necessary             Made in India Imported by:       Nova Petroleum & Chemicals Corp       3 Roethal Drive Suite 1 D       Hopewell Junction, NY 12533       www.novawax.comDistributed by:       Vini Health and Beauty Products Inc.       3 Roethal Drive Suite 1 D       Hopewell Junction, NY 12533

Which are Sofskin Petroleum UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Sofskin 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".