31645-161 NDC - MINERAL WEAR TALC FREE MINERAL AIRBRUSHING BRONZER ()

Drug Information

  • Product NDC: 31645-161
  • Proprietary Name: MINERAL WEAR TALC FREE MINERAL AIRBRUSHING BRONZER
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: PHYSICIANS FORMULA INC
Product Type:
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date:12/1/2012
End Marketing Date:1/1/2018

Package Information

No. Package Code Package Description Billing Unit
131645-161-021 CONTAINER in 1 BOX (31645-161-02) / 12 g in 1 CONTAINER (31645-161-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC31645-161Name of Company corresponding to the labeler code segment of the Product NDC.
PROPRIETARY NAMEMINERAL WEAR TALC FREE MINERAL AIRBRUSHING BRONZERThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXSPF 30A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
START MARKETING DATE12/1/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE1/1/2018This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
MARKETING CATEGORY NAMEOTC MONOGRAPH FINALAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
APPLICATION NUMBERpart352 
LABELER NAMEPHYSICIANS FORMULA INC 

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This page was last updated on: 12/6/2025

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