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  4. NDC Product Code: 98132-887 Deepest Deep

NDC 98132-887 Deepest Deep

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 98132-887?
  4. Deepest Deep 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:
98132-887
Proprietary Name:
Deepest Deep
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bare Escentuals Beauty Inc.
Labeler Code:
98132
Product Label ID:
2de9fb71-7de7-4637-852c-98bd31f40542
Start Marketing Date: [9]
01-13-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 98132-887-08

Package Description: 72 JAR in 1 CASE / 8 g in 1 JAR

Product Details

What is NDC 98132-887?

The NDC code 98132-887 is assigned by the FDA to the product Deepest Deep which is product labeled by Bare Escentuals Beauty Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 98132-887-08 72 jar in 1 case / 8 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 Deepest Deep?

Apply evenly before sun exposure as needed

Which are Deepest Deep UNII Codes?

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

Which are Deepest Deep 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".