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  4. NDC Product Code: 53407-138 Algenist

NDC 53407-138 Algenist

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 53407-138?
  4. Algenist 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:
53407-138
Proprietary Name:
Algenist
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Solazyme, Inc.
Labeler Code:
53407
Product Label ID:
4ece1847-1c94-4bf7-b936-109556a460a7
Start Marketing Date: [9]
08-01-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 53407-138-30

Package Description: 1 CARTON in 1 BOX / 1 JAR in 1 CARTON / 30 mL in 1 JAR

Product Details

What is NDC 53407-138?

The NDC code 53407-138 is assigned by the FDA to the product Algenist which is product labeled by Solazyme, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53407-138-30 1 carton in 1 box / 1 jar in 1 carton / 30 ml in 1 jar. 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 Algenist?

Shake bottle well Apply liberally to the entire face in the morning or 15 minutes prior to sun exposure Reapply at least every 2 hours Use a water resistant sunscreen if swimming or sweating Children under 6 months: Ask a doctor This lightweight fluid can be used alone, over skincare products and under makeup.

Which are Algenist UNII Codes?

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

Which are Algenist 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".