NDC 27281-011 Lung Detox

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:
27281-011
Proprietary Name:
Lung Detox
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sunway Biotech Llc
Labeler Code:
27281
Start Marketing Date: [9]
08-08-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 27281-011-96

Package Description: 30 mg in 1 BOTTLE, SPRAY

Product Details

What is NDC 27281-011?

The NDC code 27281-011 is assigned by the FDA to the product Lung Detox which is product labeled by Sunway Biotech Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 27281-011-96 30 mg in 1 bottle, spray . 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 Lung Detox?

Indications: Detoxifies the lungs and provides temporary relief from symtpoms associated with inhaling polluted air, both indoors and outdoors, such as: shortness of breath; wheezing; coughing; lack of energy.

Which are Lung Detox UNII Codes?

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

Which are Lung Detox 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".