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  4. NDC Product Code: 60193-500 Trim Men Styptic Pencil

NDC 60193-500 Trim Men Styptic Pencil

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 60193-500?
  4. Trim Men Styptic Pencil 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:
60193-500
Proprietary Name:
Trim Men Styptic Pencil
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pacific World Corporation
Labeler Code:
60193
Product Label ID:
484fe0f1-9b47-4cf2-881c-6508e9d72d3d
Start Marketing Date: [9]
11-01-2002
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 60193-500-02

Package Description: 1 CYLINDER in 1 BLISTER PACK / 28 g in 1 CYLINDER (60193-500-01)

NDC Code 60193-500-04

Package Description: 1 CYLINDER in 1 BLISTER PACK / 10 g in 1 CYLINDER (60193-500-03)

Product Details

What is NDC 60193-500?

The NDC code 60193-500 is assigned by the FDA to the product Trim Men Styptic Pencil which is product labeled by Pacific World Corporation. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 60193-500-02 1 cylinder in 1 blister pack / 28 g in 1 cylinder (60193-500-01), 60193-500-04 1 cylinder in 1 blister pack / 10 g in 1 cylinder (60193-500-03). 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 Trim Men Styptic Pencil?

Moisten tip of pencil with water and apply to affected area.Dry pencil after use.

Which are Trim Men Styptic Pencil UNII Codes?

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

Which are Trim Men Styptic Pencil 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".