NDC 64141-018 Bobbi Brown Cc Broad Spectrum Spf 25

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:
64141-018
Proprietary Name:
Bobbi Brown Cc Broad Spectrum Spf 25
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bobbi Brown Professional Cosmetics Inc.
Labeler Code:
64141
Start Marketing Date: [9]
10-01-2013
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 64141-018-01

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

Product Details

What is NDC 64141-018?

The NDC code 64141-018 is assigned by the FDA to the product Bobbi Brown Cc Broad Spectrum Spf 25 which is product labeled by Bobbi Brown Professional Cosmetics Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64141-018-01 1 tube in 1 carton / 40 ml in 1 tube. 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 Bobbi Brown Cc Broad Spectrum Spf 25?

For sunscreen use:apply liberally 15 minutes before sun exposurereapply at least every two hoursuse a water resistant sunscreen if swimming or sweatingSun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:limit time in the sun, especially from 10 a.m.-2 p.m.wear long-sleeved shirts, pants, hats and sunglasseschildren under 6 months of age: ask a doctor

Which are Bobbi Brown Cc Broad Spectrum Spf 25 UNII Codes?

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

Which are Bobbi Brown Cc Broad Spectrum Spf 25 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:

* Please review the disclaimer below.

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".