NDC 53208-502 Isa Knox 365 Sun
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 53208-502?
Which are Isa Knox 365 Sun UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Isa Knox 365 Sun 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:
- WATER (UNII: 059QF0KO0R)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- PANTHENOL (UNII: WV9CM0O67Z)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- ETHYLPARABEN (UNII: 14255EXE39)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- ACETATE ION (UNII: 569DQM74SC)
- DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
- ZINC STEARATE (UNII: H92E6QA4FV)
- CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
- FRUIT (UNII: C2AIY4ERZC)
- MARITIME PINE (UNII: 50JZ5Z98QY)
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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".