NDC 49738-557 Smart Sense Blue Mint

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:
49738-557
Proprietary Name:
Smart Sense Blue Mint
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kmart Corporation
Labeler Code:
49738
Start Marketing Date: [9]
11-26-2015
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 49738-557-02

Package Description: 3000 mL in 1 BOTTLE, PLASTIC

NDC Code 49738-557-16

Package Description: 500 mL in 1 BOTTLE, PLASTIC

NDC Code 49738-557-17

Package Description: 500 mL in 1 BOTTLE, PLASTIC

NDC Code 49738-557-33

Package Description: 1000 mL in 1 BOTTLE, PLASTIC

NDC Code 49738-557-34

Package Description: 1000 mL in 1 BOTTLE, PLASTIC

NDC Code 49738-557-51

Package Description: 1500 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 49738-557?

The NDC code 49738-557 is assigned by the FDA to the product Smart Sense Blue Mint which is product labeled by Kmart Corporation. The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 49738-557-02 3000 ml in 1 bottle, plastic , 49738-557-16 500 ml in 1 bottle, plastic , 49738-557-17 500 ml in 1 bottle, plastic , 49738-557-33 1000 ml in 1 bottle, plastic , 49738-557-34 1000 ml in 1 bottle, plastic , 49738-557-51 1500 ml 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 Smart Sense Blue Mint?

Rinse full strength for 30 seconds with 20 mL (2/3 fluid ounce or 4 teaspoonfuls) morning and nightDo not swallow

Which are Smart Sense Blue Mint UNII Codes?

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

Which are Smart Sense Blue Mint 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:

What is the NDC to RxNorm Crosswalk for Smart Sense Blue Mint?

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:
  • RxCUI: 1043619 - eucalyptol 0.092 % / menthol 0.042 % / methyl salicylate 0.06 % / thymol 0.064 % Mouthwash
  • RxCUI: 1043619 - eucalyptol 0.92 MG/ML / menthol 0.42 MG/ML / methyl salicylate 0.6 MG/ML / thymol 0.64 MG/ML Mouthwash

* Please review the disclaimer below.

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".