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  4. NDC Product Code: 49738-563 Smart Sense Sinus And Headache

NDC 49738-563 Smart Sense Sinus And Headache

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 49738-563?
  5. Smart Sense Sinus And Headache Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
49738-563
Proprietary Name:
Smart Sense Sinus And Headache
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kmart Corporation
Labeler Code:
49738
Product Label ID:
6bfd2de7-28be-4889-9ea4-36749469bc39
Start Marketing Date: [9]
04-05-2017
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)
Shape:
CAPSULE (C48336)
Size(s):
16 MM
Imprint(s):
L272
Score:
1
Flavor(s):
VANILLA (C73421 - MENTHOL)

Code Structure Chart

Product Details

What is NDC 49738-563?

The NDC code 49738-563 is assigned by the FDA to the product Smart Sense Sinus And Headache which is product labeled by Kmart Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49738-563-62 12 blister pack in 1 carton / 2 tablet, film coated in 1 blister pack. 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 Sinus And Headache?

•do not take more than directed (see overdose warning)adults and children 12 years and over•take 2 caplets every 4 hours•swallow whole – do not crush, chew or dissolve•do not take more than 10 caplets in 24 hourschildren under 12 yearsask a doctor

Which are Smart Sense Sinus And Headache UNII Codes?

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

Which are Smart Sense Sinus And Headache 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 Sinus And Headache?

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: 1046378 - acetaminophen 325 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1046378 - acetaminophen 325 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1046378 - APAP 325 MG / phenylephrine hydrochloride 5 MG Oral Tablet

* 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".