NDC 64141-030 Skin Long-wear Fluid Powder Foundation Broad Spectrum Spf 20

Ensulizole, Titanium Dioxide, And Zinc Oxide

NDC Product Code 64141-030

NDC Code: 64141-030

Proprietary Name: Skin Long-wear Fluid Powder Foundation Broad Spectrum Spf 20 What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Ensulizole, Titanium Dioxide, And Zinc Oxide What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 64141 - Bobbi Brown Professional Cosmetics Inc.
    • 64141-030 - Skin Long-wear Fluid Powder Foundation Broad Spectrum Spf 20

NDC 64141-030-01

Package Description: 1 TUBE in 1 CARTON > 40 mL in 1 TUBE

NDC Product Information

Skin Long-wear Fluid Powder Foundation Broad Spectrum Spf 20 with NDC 64141-030 is a a human over the counter drug product labeled by Bobbi Brown Professional Cosmetics Inc.. The generic name of Skin Long-wear Fluid Powder Foundation Broad Spectrum Spf 20 is ensulizole, titanium dioxide, and zinc oxide. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Bobbi Brown Professional Cosmetics Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Skin Long-wear Fluid Powder Foundation Broad Spectrum Spf 20 Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ENSULIZOLE .022 g/mL
  • TITANIUM DIOXIDE .041 g/mL
  • ZINC OXIDE .02 g/mL

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Bobbi Brown Professional Cosmetics Inc.
Labeler Code: 64141
FDA Application Number: part352 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product 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.

Start Marketing Date: 10-16-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

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Skin Long-wear Fluid Powder Foundation Broad Spectrum Spf 20 Product Label Images