NDC 64942-0034 Vaseline Pure

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:
64942-0034
Proprietary Name:
Vaseline Pure
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Conopco Inc. D/b/a Unilever
Labeler Code:
64942
Start Marketing Date: [9]
03-18-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 64942-0034-1

Package Description: 49 g in 1 JAR

NDC Code 64942-0034-2

Package Description: 71 g in 1 TUBE

NDC Code 64942-0034-3

Package Description: 106 g in 1 JAR

NDC Code 64942-0034-4

Package Description: 212 g in 1 JAR

NDC Code 64942-0034-5

Package Description: 368 g in 1 JAR

Product Details

What is NDC 64942-0034?

The NDC code 64942-0034 is assigned by the FDA to the product Vaseline Pure which is product labeled by Conopco Inc. D/b/a Unilever. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 64942-0034-1 49 g in 1 jar , 64942-0034-2 71 g in 1 tube , 64942-0034-3 106 g in 1 jar , 64942-0034-4 212 g in 1 jar , 64942-0034-5 368 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 Vaseline Pure?

Uses■ temporarily protects minor ●cuts ●scrapes ●burns■ temporarily protects and helps relieve chapped or cracked skin and lips■ helps protect from the drying effects of wind and cold weather

Which are Vaseline Pure UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Vaseline Pure?

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".