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  4. NDC Product Code: 33992-0621 Nitetime Multi-symptom Cold/flu Relief

NDC 33992-0621 Nitetime 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 33992-0621?
  5. Nitetime 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:
33992-0621
Proprietary Name:
Nitetime Multi-symptom Cold/flu Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Greenbrier International
Labeler Code:
33992
Product Label ID:
e278b8ad-2eb0-4bd8-a455-a8a438e87f97
Start Marketing Date: [9]
01-04-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)
Shape:
OVAL (C48345)
Size(s):
21 MM
Imprint(s):
RP062
Score:
1

Code Structure Chart

Product Details

What is NDC 33992-0621?

The NDC code 33992-0621 is assigned by the FDA to the product Nitetime Multi-symptom Cold/flu Relief which is product labeled by Greenbrier International. The product's dosage form is . The product is distributed in a single package with assigned NDC code 33992-0621-0 1 blister pack in 1 carton / 10 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 Nitetime Multi-symptom Cold/flu Relief?

Take only as directed - see Overdose warningdo not exceed 4 doses per 24 hrsAdults & children 12 years and over2 softgels with water every 6 hrsChildren 4 to under 12 yearsask a doctorChildren under 4 yearsdo not use

Which are Nitetime Multi-symptom Cold/flu Relief UNII Codes?

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

Which are Nitetime 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 Nitetime 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: 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
  • RxCUI: 1094549 - APAP 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".