NDC 44717-538 Natria Brightening Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 44717-538?
What are the uses for Natria Brightening Spf 15?
Which are Natria Brightening Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Natria Brightening Spf 15 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:
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- ISOPENTYLDIOL (UNII: 19NOL5474Q)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- SQUALENE (UNII: 7QWM220FJH)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
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[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".