NDC 46084-121 Daytime Nighttime Cold/flu Relief A P J

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:
46084-121
Proprietary Name:
Daytime Nighttime Cold/flu Relief A P J
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
A P J Laboratories Limited
Labeler Code:
46084
Start Marketing Date: [9]
06-01-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328 - LIGHT YELLOWISH PINK)
WHITE (C48325)
Shape:
OVAL (C48345)
Size(s):
20 MM
Imprint(s):
425MG
Score:
2

Product Packages

NDC Code 46084-121-01

Package Description: 1 KIT in 1 PACKAGE * 20 TABLET in 1 BLISTER PACK (46084-122-20) * 20 TABLET in 1 BLISTER PACK (46084-123-20)

Product Details

What is NDC 46084-121?

The NDC code 46084-121 is assigned by the FDA to the product Daytime Nighttime Cold/flu Relief A P J which is product labeled by A P J Laboratories Limited. The product's dosage form is . The product is distributed in a single package with assigned NDC code 46084-121-01 1 kit in 1 package * 20 tablet in 1 blister pack (46084-122-20) * 20 tablet in 1 blister pack (46084-123-20). 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 Daytime Nighttime Cold/flu Relief A P J?

•take only as directed – see Overdose warning •take Nighttime OR Daytime.Nighttime tablets •do not exceed 4 doses per 24 hours adults and children 12 years and over  swallow 2 softgels with water every 6 hrs  children 4 to under 12 years  ask a doctor  children under 4 years  do not use DayTime tablets •do not exceed 4 doses per 24 hours adults and children 12 years and over  swallow 2 softgels with water every 4 hrs  children 4 to under 12 years  ask a doctor  children under 4 years  do not use •when using other Daytime or Nighttime products, carefully read each label to insure correct dosing

Which are Daytime Nighttime Cold/flu Relief A P J UNII Codes?

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

Which are Daytime Nighttime Cold/flu Relief A P J 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 Daytime Nighttime Cold/flu Relief A P J?

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: 1094538 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1094538 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1094538 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1425315 - acetaminophen 325 MG / chlorpheniramine maleate 6.25 MG / dextromethorphan HBr 15 MG Oral Tablet
  • RxCUI: 1425315 - acetaminophen 325 MG / chlorpheniramine maleate 6.25 MG / dextromethorphan hydrobromide 15 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".