NDC 64141-001 Bobbi Brown Skin Foundation Spf 15

  1. Labeler Index
  2. Bobbi Brown Professional Cosmetics Inc
  3. NDC: 64141-001 Bobbi Brown Skin Foundation Spf 15

NDC Product Code 64141-001

NDC CODE: 64141-001

Proprietary Name: Bobbi Brown Skin Foundation Spf 15 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.

NDC Code Structure

NDC 64141-001-01

Package Description: 1 BOTTLE, GLASS in 1 CARTON > 30 mL in 1 BOTTLE, GLASS (64141-001-02)

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Bobbi Brown Skin Foundation Spf 15 with NDC 64141-001 is a product labeled by Bobbi Brown Professional Cosmetics Inc. The product's dosage form is and is administered via form.

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
Start Marketing Date: 06-01-2008 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: 12-31-2017 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

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Bobbi Brown Skin Foundation Spf 15 Product Label Images

Bobbi Brown Skin Foundation Spf 15 Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

ACTIVE INGREDIENTS: 7.5% OCTINOXATE, 1.0% TITANIUM DIOXIDE

Otc - Purpose

INDICATIONS: PROVIDES BROAD SPECTRUM PROTECTION FROM SUN'S DAMAGING RAYS.USAGE: SHAKE WELL BEFORE USE. APPLY PRIOR TO SUN EXPOSURE

Warnings

WARNING:KEEP OUT OF EYES. STOP USE IF IRRITATION OCCURS. KEEP OUT OF REACH OF CHILDREN.

* Please review the disclaimer below.