44924-132 NDC - DR. BABOR PURITY CELLULAR ULTIMATE BLEMISH REDUCING DUO ()

Drug Information

  • Product NDC: 44924-132
  • Proprietary Name: Dr. Babor Purity Cellular Ultimate Blemish Reducing Duo
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Babor Cosmetics America, Corp.
Product Type:
FDA Application Number: part333D
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date:7/31/2013
End Marketing Date:2/17/2017

Package Information

No. Package Code Package Description Billing Unit
144924-132-011 KIT in 1 KIT (44924-132-01) / 1 KIT in 1 KIT

NDC Record

Field Name Field Value Definition
PRODUCT NDC44924-132The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAMEDr. Babor Purity Cellular Ultimate Blemish Reducing DuoThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/31/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE2/17/2017Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
MARKETING CATEGORY NAMEOTC MONOGRAPH FINALProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERpart333DName of Company corresponding to the labeler code segment of the Product NDC.
LABELER NAMEBabor Cosmetics America, Corp.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 12/19/2025

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