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  4. NDC Product Code: 61509-100 Hemostat

NDC 61509-100 Hemostat

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 61509-100?
  5. Hemostat 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:
61509-100
Proprietary Name:
Hemostat
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cargus International, Inc.
Labeler Code:
61509
Product Label ID:
ddb206ac-28ed-48ac-8d78-88e95cf03918
Start Marketing Date: [9]
03-01-2013
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - COLORLESS)

Code Structure Chart

Product Details

What is NDC 61509-100?

The NDC code 61509-100 is assigned by the FDA to the product Hemostat which is product labeled by Cargus International, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61509-100-18 30 ml in 1 bottle, plastic . 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 Hemostat?

Soak a cotton tipped applicator with Hemostat. Apply to bleeding area with pressure until bleeding is stopped. Should a small dark coagulum appear, flush it away with water. This will have no effect on hemostatic action. Remove the impregnated cord from sulcus. Flush with water and dry with air. If hemostasis is not achieved, repeat application, rinse with water and air dry until bleeding is no longer present.

Which are Hemostat UNII Codes?

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

Which are Hemostat 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 Hemostat?

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: 966557 - aluminum chloride 25 % Mucous Membrane Topical Solution
  • RxCUI: 966557 - aluminum chloride 250 MG/ML Mucous Membrane Topical Solution
  • RxCUI: 966557 - aluminum chloride 7500 MG in 30 ML Mucous Membrane Topical 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".