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  4. NDC Product Code: 67510-0523 Day Time Gelcap

NDC 67510-0523 Day Time Gelcap

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 67510-0523?
  5. Day Time Gelcap 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:
67510-0523
Proprietary Name:
Day Time Gelcap
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kareway Product, Inc.
Labeler Code:
67510
Product Label ID:
4e73c368-e4eb-471e-aca4-fe551bde52bf
Start Marketing Date: [9]
06-01-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331)
Shape:
CAPSULE (C48336)
Size(s):
24 MM
Imprint(s):
DYTIME
Score:
1

Product Packages

NDC Code 67510-0523-0

Package Description: 2 BLISTER PACK in 1 BOX / 20 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Code 67510-0523-1

Package Description: 1 BLISTER PACK in 1 BOX / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Code 67510-0523-2

Package Description: 1 BLISTER PACK in 1 BOX / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Code 67510-0523-4

Package Description: 2 BLISTER PACK in 1 BOX / 24 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Product Details

What is NDC 67510-0523?

The NDC code 67510-0523 is assigned by the FDA to the product Day Time Gelcap which is product labeled by Kareway Product, Inc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 67510-0523-0 2 blister pack in 1 box / 20 capsule, liquid filled in 1 blister pack, 67510-0523-1 1 blister pack in 1 box / 10 capsule, liquid filled in 1 blister pack, 67510-0523-2 1 blister pack in 1 box / 12 capsule, liquid filled in 1 blister pack, 67510-0523-4 2 blister pack in 1 box / 24 capsule, liquid filled 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 Gelcap?

Take only as directed-see Overdose warningdo not exceed 4 doses per 24 hoursadults and children 12 yrs and over2 GelCaps with water every 6 hrschildren 4 to under 12 yrsask a doctorchildren under 4 yrsdo not use

Which are Day Time Gelcap UNII Codes?

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

Which are Day Time Gelcap 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 Gelcap?

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

* 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".