NDC 0363-6040 Medicated Lip Balm

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:
0363-6040
Proprietary Name:
Medicated Lip Balm
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Walgreen Co
Labeler Code:
0363
Start Marketing Date: [9]
10-30-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 0363-6040-02

Package Description: 2 JAR in 1 BLISTER PACK / 7 g in 1 JAR (0363-6040-01)

Product Details

What is NDC 0363-6040?

The NDC code 0363-6040 is assigned by the FDA to the product Medicated Lip Balm which is product labeled by Walgreen Co. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0363-6040-02 2 jar in 1 blister pack / 7 g in 1 jar (0363-6040-01). 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 Medicated Lip Balm?

Adults and children 2 years of age and older, apply to lips not more than 3 to 4 times dailychildren under 2 years of age: ask a doctor

Which are Medicated Lip Balm UNII Codes?

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

Which are Medicated Lip Balm 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:

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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".