NDC 13537-402 Lbel Uv Defense 365
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 13537-402?
What are the uses for Lbel Uv Defense 365?
Which are Lbel Uv Defense 365 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Lbel Uv Defense 365 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)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARETH-12 (UNII: 7V4MR24V5P)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- AMBROSIA PERUVIANA LEAF (UNII: 458F79CGBF)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- MICA (UNII: V8A1AW0880)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SUNFLOWER SEED (UNII: R9N3379M4Z)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- HEDERA HELIX TOP (UNII: 379040L9FW)
- PHYTIC ACID (UNII: 7IGF0S7R8I)
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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".