NDC 98132-725 Bareminerals Blemish Therapy

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
98132-725
Proprietary Name:
Bareminerals Blemish Therapy
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
98132
Start Marketing Date: [9]
12-31-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 98132-725?

The NDC code 98132-725 is assigned by the FDA to the product Bareminerals Blemish Therapy 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 98132-725-01 1 jar in 1 carton / 1 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 Bareminerals Blemish Therapy?

USE FOR THE TREATMENT OF ACNE. CLEARS ACNE BLEMISHES AND ALLOWS SKIN TO HEAL. PENETRATES PORES TO CONTROL BLACKHEADS. HELPS PREVENT NEW ACNE BLEMISHES FROM FORMING.

Which are Bareminerals Blemish Therapy UNII Codes?

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

Which are Bareminerals Blemish Therapy 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 Bareminerals Blemish Therapy?

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:

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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".