1. Home
  2. Labeler Index
  3. Borisovskiy Zavod Medicinskikh Preparatov Jsc
  4. NDC Product Code: 16638-042 Balsamic Liniment

NDC 16638-042 Balsamic Liniment

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 16638-042?
  5. Balsamic Liniment 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:
16638-042
Proprietary Name:
Balsamic Liniment
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Borisovskiy Zavod Medicinskikh Preparatov Jsc
Labeler Code:
16638
Product Label ID:
2a001d2e-f076-4bfc-a61c-c8f8d8044fea
Start Marketing Date: [9]
12-22-2000
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332 - FROM LIGHT BROWN TO GREEN-BROWN)

Code Structure Chart

Product Details

What is NDC 16638-042?

The NDC code 16638-042 is assigned by the FDA to the product Balsamic Liniment which is product labeled by Borisovskiy Zavod Medicinskikh Preparatov Jsc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 16638-042-42 40 g in 1 package . 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 Balsamic Liniment?

Apply to affected areas one to two times daily or as directed by physician.

Which are Balsamic Liniment UNII Codes?

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

Which are Balsamic Liniment 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".