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  4. NDC Product Code: 81376-212 Urea 40 Plus Sa

NDC 81376-212 Urea 40 Plus Sa

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 81376-212?
  5. Urea 40 Plus Sa 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:
81376-212
Proprietary Name:
Urea 40 Plus Sa
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ssg Ventures Inc
Labeler Code:
81376
Product Label ID:
b7114c78-d92c-5c7a-e053-2995a90a63e3
Start Marketing Date: [9]
09-20-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - OPAQUE WHITE)

Product Packages

NDC Code 81376-212-01

Package Description: 113 g in 1 JAR

Product Details

What is NDC 81376-212?

The NDC code 81376-212 is assigned by the FDA to the product Urea 40 Plus Sa which is product labeled by Ssg Ventures Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81376-212-01 113 g in 1 jar . 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 Urea 40 Plus Sa?

SOOTHES ROUGH & DRY SKIN

Which are Urea 40 Plus Sa UNII Codes?

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

Which are Urea 40 Plus Sa 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".