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  4. NDC Product Code: 68210-1480 N - Time Sinus

NDC 68210-1480 N - Time Sinus

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 68210-1480?
  5. N - Time Sinus 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:
68210-1480
Proprietary Name:
N - Time Sinus
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Spirit Pharmaceuticals,llc
Labeler Code:
68210
Product Label ID:
e3be9ee0-b9bb-4a09-a40a-dbe2f08325ad
Start Marketing Date: [9]
03-01-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)
Shape:
OVAL (C48345)
Size(s):
18 MM
Imprint(s):
130
Score:
1

Code Structure Chart

Product Details

What is NDC 68210-1480?

The NDC code 68210-1480 is assigned by the FDA to the product N - Time Sinus which is product labeled by Spirit Pharmaceuticals,llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 68210-1480-5 5000 capsule, liquid filled in 1 drum , 68210-1480-6 6000 capsule, liquid filled in 1 drum . 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 N - Time Sinus?

Take only as recommended - see Overdose warningdo not exceed 6 doses per 24 hoursNyQuil Sinus OR DayQuil Sinusadults and children 12 years and over2 LiquiCaps with water every 4 hourschildren 2 to under 12 years ask a doctorchildren under 2 yearsdo not usewhen using other DayQuil or NyQuil products, carefully read each label to insure correct dosing

Which are N - Time Sinus UNII Codes?

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

Which are N - Time Sinus 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 N - Time Sinus?

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: 1052647 - acetaminophen 325 MG / doxylamine succinate 6.25 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1052647 - acetaminophen 325 MG / doxylamine succinate 6.25 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1052647 - APAP 325 MG / doxylamine succinate 6.25 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".