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  4. NDC Product Code: 68016-146 Night-time Cherry Multi-symptom Cold/flu Relief

NDC 68016-146 Night-time Cherry Multi-symptom Cold/flu Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 68016-146?
  5. Night-time Cherry Multi-symptom Cold/flu Relief 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:
68016-146
Proprietary Name:
Night-time Cherry Multi-symptom Cold/flu Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Chain Drug Consortium, Llc
Labeler Code:
68016
Product Label ID:
c45fafda-15d9-40d2-bf95-517f11a729cf
Start Marketing Date: [9]
09-01-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
CHERRY (C73375 - CHERRY)

Product Packages

NDC Code 68016-146-00

Package Description: 236 mL in 1 BOTTLE

NDC Code 68016-146-01

Package Description: 354 mL in 1 BOTTLE

Product Details

What is NDC 68016-146?

The NDC code 68016-146 is assigned by the FDA to the product Night-time Cherry Multi-symptom Cold/flu Relief which is product labeled by Chain Drug Consortium, Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 68016-146-00 236 ml in 1 bottle , 68016-146-01 354 ml 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 Night-time Cherry Multi-symptom Cold/flu Relief?

Take only as recommended-see Overdose warningsUse dose cup or tablespoon (TBSP)do not exceed 4 doses per 24 hoursIf taking Night Time at night and Day Time during the day, limit total to 4 doses per 24 hours

Which are Night-time Cherry Multi-symptom Cold/flu Relief UNII Codes?

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

Which are Night-time Cherry Multi-symptom Cold/flu Relief 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 Night-time Cherry Multi-symptom Cold/flu Relief?

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: 1043400 - acetaminophen 650 MG / dextromethorphan HBr 30 MG / doxylamine succinate 12.5 MG in 30 mL Oral Solution
  • RxCUI: 1043400 - acetaminophen 21.7 MG/ML / dextromethorphan hydrobromide 1 MG/ML / doxylamine succinate 0.417 MG/ML Oral Solution
  • RxCUI: 1043400 - acetaminophen 325 MG / dextromethorphan HBr 15 MG / doxylamine succinate 6.25 MG per 15 ML Oral Solution
  • RxCUI: 1043400 - acetaminophen 650 MG / dextromethorphan HBr 30 MG / doxylamine succinate 12.5 MG per 30 ML Oral Solution
  • RxCUI: 1043400 - APAP 21.7 MG/ML / Dextromethorphan Hydrobromide 1 MG/ML / doxylamine succinate 0.417 MG/ML Oral Solution

* 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".