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  4. NDC Product Code: 11697-372 Flawless By Sonya Aloe Bb Creme Sandy

NDC 11697-372 Flawless By Sonya Aloe Bb Creme Sandy

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 11697-372?
  4. Flawless By Sonya Aloe Bb Creme Sandy 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:
11697-372
Proprietary Name:
Flawless By Sonya Aloe Bb Creme Sandy
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Aloe Vera Of America, Inc.
Labeler Code:
11697
Product Label ID:
e2bd982e-3e5b-4857-9af0-087abe92de9f
Start Marketing Date: [9]
01-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 11697-372?

The NDC code 11697-372 is assigned by the FDA to the product Flawless By Sonya Aloe Bb Creme Sandy which is product labeled by Aloe Vera Of America, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11697-372-02 1 tube in 1 carton / 45 g in 1 tube (11697-372-01). 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 Flawless By Sonya Aloe Bb Creme Sandy?

Other informationprotect the product in the enclosed container from excessive heat and direct sunFor your protection, this carton has a clear safety seal on both top and bottom flaps

Which are Flawless By Sonya Aloe Bb Creme Sandy UNII Codes?

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

Which are Flawless By Sonya Aloe Bb Creme Sandy 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".