NDC 76173-1001 Rendrevie Sun Screen Spf35 Pa
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 76173-1001?
What are the uses for Rendrevie Sun Screen Spf35 Pa?
Which are Rendrevie Sun Screen Spf35 Pa UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Rendrevie Sun Screen Spf35 Pa 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- TALC (UNII: 7SEV7J4R1U)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
- MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)
- ALGELDRATE (UNII: 03J11K103C)
- ALUMINUM STEARATE (UNII: U6XF9NP8HM)
- IMIDUREA (UNII: M629807ATL)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CHAMOMILE (UNII: FGL3685T2X)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- SQUALANE (UNII: GW89575KF9)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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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".