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  4. NDC Product Code: 50114-3250 Sinusin

NDC 50114-3250 Sinusin

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50114-3250?
  4. Sinusin Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50114-3250
Proprietary Name:
Sinusin
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Heel Inc
Labeler Code:
50114
Product Label ID:
ffc639db-ba39-49ef-97c6-df2cb1a86ed4
Start Marketing Date: [9]
01-31-2007
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 50114-3250?

The NDC code 50114-3250 is assigned by the FDA to the product Sinusin which is product labeled by Heel Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50114-3250-4 50 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 Sinusin?

For the temporary relief of:Nasal CongestionRhinitis and SinusitisCold and Flu Nasal Symptoms

Which are Sinusin UNII Codes?

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

  • PULSATILLA VULGARIS (UNII: I76KB35JEV)
  • PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
  • EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K)
  • EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K) (Active Moiety)
  • LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU)
  • LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU) (Active Moiety)
  • MERCURIC IODIDE (UNII: R03O05RB0P)
  • MERCURIC IODIDE (UNII: R03O05RB0P) (Active Moiety)
  • SILVER NITRATE (UNII: 95IT3W8JZE)
  • SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
  • CALCIUM SULFIDE (UNII: 1MBW07J51Q)
  • CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
  • SINUSITISINUM (UNII: B575563DM5)
  • SINUSITISINUM (UNII: B575563DM5) (Active Moiety)
  • INFLUENZA A VIRUS A/SINGAPORE/6/86 (H1N1) HEMAGGLUTININ ANTIGEN (HEAT INACTIVATED) (UNII: DRA5YV248Q)
  • INFLUENZA A VIRUS A/SINGAPORE/6/86 (H1N1) HEMAGGLUTININ ANTIGEN (HEAT INACTIVATED) (UNII: DRA5YV248Q) (Active Moiety)
  • INFLUENZA A VIRUS A/BEIJING/32/92 (H3N2) HEMAGGLUTININ ANTIGEN (HEAT INACTIVATED) (UNII: 0835GZ42BC)
  • INFLUENZA A VIRUS A/BEIJING/32/92 (H3N2) HEMAGGLUTININ ANTIGEN (HEAT INACTIVATED) (UNII: 0835GZ42BC) (Active Moiety)
  • INFLUENZA B VIRUS B/PANAMA/45/90 HEMAGGLUTININ ANTIGEN (HEAT INACTIVATED) (UNII: 790PSW8427)
  • INFLUENZA B VIRUS B/PANAMA/45/90 HEMAGGLUTININ ANTIGEN (HEAT INACTIVATED) (UNII: 790PSW8427) (Active Moiety)

Which are Sinusin 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:

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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".