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  4. NDC Product Code: 68391-490 Daytime Nighttime Cold/flu

NDC 68391-490 Daytime Nighttime Cold/flu

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 68391-490?
  5. Daytime Nighttime Cold/flu 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:
68391-490
Proprietary Name:
Daytime Nighttime Cold/flu
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bjwc (berkley & Jensen / Bj's)
Labeler Code:
68391
Product Label ID:
9ced5c93-4deb-4e55-b92d-227fd3e3079d
Start Marketing Date: [9]
01-15-2013
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331)
GREEN (C48329)
Shape:
CAPSULE (C48336)
Size(s):
20 MM
Imprint(s):
P19;95A;36A
P30;94A;35A
Score:
1

Code Structure Chart

Product Details

What is NDC 68391-490?

The NDC code 68391-490 is assigned by the FDA to the product Daytime Nighttime Cold/flu which is product labeled by Bjwc (berkley & Jensen / Bj's). The product's dosage form is . The product is distributed in a single package with assigned NDC code 68391-490-72 1 kit in 1 carton * 12 capsule in 1 blister pack * 12 capsule 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 Daytime Nighttime Cold/flu?

Do not take more than directed (see overdose warning)do not take more than 4 doses in 24 hours swallow whole: do not crush, chew, or dissolve Daytime: adults and children 12 years and over: take 2 softgels with water every 4 hours Nighttime: adults and children 12 years and over: take 2 softgels with water every 6 hours children under 12 years: do not use

Which are Daytime Nighttime Cold/flu UNII Codes?

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

Which are Daytime Nighttime Cold/flu 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?

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: 1086997 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1086997 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1094549 - acetaminophen 325 MG / dextromethorphan HBr 15 MG / doxylamine succinate 6.25 MG Oral Capsule
  • RxCUI: 1094549 - acetaminophen 325 MG / dextromethorphan hydrobromide 15 MG / doxylamine succinate 6.25 MG Oral Capsule

* 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".