NDC 52000-003 Allure Vaporizing Chest Rub

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:
52000-003
Proprietary Name:
Allure Vaporizing Chest Rub
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
52000
Start Marketing Date: [9]
06-30-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 52000-003?

The NDC code 52000-003 is assigned by the FDA to the product Allure Vaporizing Chest Rub which is product labeled by Universal Distribution Center Llc. The product's dosage form is . The product is distributed in 7 packages with assigned NDC codes 52000-003-08 50 g in 1 bottle, plastic , 52000-003-09 56.6 g in 1 bottle, plastic , 52000-003-10 100 g in 1 bottle, plastic , 52000-003-11 113 g in 1 bottle, plastic , 52000-003-12 150 g in 1 bottle, plastic , 52000-003-13 170 g in 1 bottle, plastic , 52000-003-14 226 g in 1 bottle, plastic . 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 Allure Vaporizing Chest Rub?

Adults and children 2 years and overrub a thick layer on chest and throat or rub on sore aching muscles repeat up to 3 times per 24 hours or as directed by doctordo not use on children under 2 years unless directed by doctor

Which are Allure Vaporizing Chest Rub UNII Codes?

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

Which are Allure Vaporizing Chest Rub 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".