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  4. NDC Product Code: 68016-490 Day-time Night-time

NDC 68016-490 Day-time Night-time

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 68016-490?
  5. Day-time Night-time 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:
68016-490
Proprietary Name:
Day-time Night-time
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Chain Drug Consortium, Llc
Labeler Code:
68016
Product Label ID:
40033873-4d75-407d-a9a4-851216178c0e
Start Marketing Date: [9]
07-12-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

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

Code Structure Chart

Product Details

What is NDC 68016-490?

The NDC code 68016-490 is assigned by the FDA to the product Day-time Night-time which is product labeled by Chain Drug Consortium, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 68016-490-40 1 kit in 1 carton * 10 capsule in 1 blister pack * 10 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 Day-time Night-time?

Take only as recommended (see overdose warning)take Night-Time or Day-Time age Night-Time Day-Time adults and children 12 years of age and older swallow 2 softgels with water every 6 hours swallow 2 softgels with water every 4 hours children 4 to 12 years of age ask a doctor ask a doctor children under 4 years of age do not use do not useIf taking Night-Time and Day-Time softgels limit total to 4 doses per day

Which are Day-time Night-time UNII Codes?

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

Which are Day-time Night-time 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 Day-time Night-time?

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".