NDC 72208-352 The Ordinary Suncare Mineral Uv Filters With Antioxidants Spf30

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:
72208-352
Proprietary Name:
The Ordinary Suncare Mineral Uv Filters With Antioxidants Spf30
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Deciem Inc
Labeler Code:
72208
Start Marketing Date: [9]
05-18-2018
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72208-352-04

Package Description: 1 TUBE in 1 CARTON / 50 mL in 1 TUBE (72208-352-01)

Product Details

What is NDC 72208-352?

The NDC code 72208-352 is assigned by the FDA to the product The Ordinary Suncare Mineral Uv Filters With Antioxidants Spf30 which is product labeled by Deciem Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72208-352-04 1 tube in 1 carton / 50 ml in 1 tube (72208-352-01). 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 The Ordinary Suncare Mineral Uv Filters With Antioxidants Spf30?

  apply liverally and evenly to face 15 minutes before sun exposue  for children under 6 months of age: Ask a doctor prior to use.​Reapply​Reapply at lease every 2 hours use a water resistant sunscreen if swimming or sweating 

Which are The Ordinary Suncare Mineral Uv Filters With Antioxidants Spf30 UNII Codes?

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

Which are The Ordinary Suncare Mineral Uv Filters With Antioxidants Spf30 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".