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  4. NDC Product Code: 57520-0134 Sinus Clear

NDC 57520-0134 Sinus Clear

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 57520-0134?
  5. Sinus Clear Uses
  6. Active Ingredients UNII Codes
  7. 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:
57520-0134
Proprietary Name:
Sinus Clear
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Apotheca Company
Labeler Code:
57520
Product Label ID:
bef88764-f5f2-4bb0-b7c0-5fb0b20fa137
Start Marketing Date: [9]
11-04-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - NATURAL VEGETABLE)
Shape:
CAPSULE (C48336)
Size(s):
25 MM
Imprint(s):
NONE
Score:
1

Product Packages

NDC Code 57520-0134-1

Package Description: 60 CAPSULE in 1 CONTAINER

Product Details

What is NDC 57520-0134?

The NDC code 57520-0134 is assigned by the FDA to the product Sinus Clear which is product labeled by Apotheca Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 57520-0134-1 60 capsule in 1 container . 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 Sinus Clear?

SINUS CLEAR is a carefully formulated homeopathic remedy which effectively relieves nasal congestion an restores free breathing through the nose.  Sinus Clear is non-drowsy and produces no side effects.

Which are Sinus Clear UNII Codes?

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

Which are Sinus Clear 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:

* 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".