NDC 49738-184 Headache Relief Extra Strength

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:
49738-184
Proprietary Name:
Headache Relief Extra Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Smart Sense (kmart)
Labeler Code:
49738
Start Marketing Date: [9]
06-19-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
CAPSULE (C48336)
Size(s):
17 MM
Imprint(s):
2793
Score:
1

Product Packages

NDC Code 49738-184-10

Package Description: 1 BOTTLE in 1 BOX / 100 TABLET in 1 BOTTLE

NDC Code 49738-184-20

Package Description: 1 BOTTLE in 1 BOX / 200 TABLET in 1 BOTTLE

NDC Code 49738-184-50

Package Description: 1 BOTTLE in 1 BOX / 50 TABLET in 1 BOTTLE

Product Details

What is NDC 49738-184?

The NDC code 49738-184 is assigned by the FDA to the product Headache Relief Extra Strength which is product labeled by Smart Sense (kmart). The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 49738-184-10 1 bottle in 1 box / 100 tablet in 1 bottle, 49738-184-20 1 bottle in 1 box / 200 tablet in 1 bottle, 49738-184-50 1 bottle in 1 box / 50 tablet in 1 bottle. 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 Headache Relief Extra Strength?

Do not use more than directed drink a full glass of water with each dose adults and children 12 years and over: take 2 caplets every 6 hours; not more than 8 caplets in 24 hours children under 12 years: ask a doctor

Which are Headache Relief Extra Strength UNII Codes?

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

Which are Headache Relief Extra Strength 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 Headache Relief Extra Strength?

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: 308297 - acetaminophen 250 MG / aspirin 250 MG / caffeine 65 MG Oral Tablet
  • RxCUI: 308297 - APAP 250 MG / ASA 250 MG / caffeine 65 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".