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NDC 76049-121 Jane Be Beautiful Multi-benefit Bb Broad Spectrum Spf 30 Dark

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 76049-121?
  4. Jane Be Beautiful Multi-benefit Bb Broad Spectrum Spf 30 Dark Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
76049-121
Proprietary Name:
Jane Be Beautiful Multi-benefit Bb Broad Spectrum Spf 30 Dark
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Stila Styles
Labeler Code:
76049
Product Label ID:
37154826-c34a-416d-a9a3-5004156dccd6
Start Marketing Date: [9]
10-31-2013
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 76049-121?

The NDC code 76049-121 is assigned by the FDA to the product Jane Be Beautiful Multi-benefit Bb Broad Spectrum Spf 30 Dark which is product labeled by Stila Styles. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76049-121-01 30 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 Jane Be Beautiful Multi-benefit Bb Broad Spectrum Spf 30 Dark?

For sunscreen use:apply liberally 15 minutes before sun exposurereapply at least every 2 hoursuse water resistant sunscreen if swimming or sweating

Which are Jane Be Beautiful Multi-benefit Bb Broad Spectrum Spf 30 Dark UNII Codes?

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

Which are Jane Be Beautiful Multi-benefit Bb Broad Spectrum Spf 30 Dark 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:

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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".