NDC 43455-0001 Lbel Defense 365 Daily Protective Facial Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 43455-0001?
What are the uses for Lbel Defense 365 Daily Protective Facial Spf 50?
Which are Lbel Defense 365 Daily Protective Facial Spf 50 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 Defense 365 Daily Protective Facial Spf 50 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)
- ALCOHOL (UNII: 3K9958V90M)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- CETEARETH-12 (UNII: 7V4MR24V5P)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- AMBROSIA PERUVIANA LEAF (UNII: 458F79CGBF)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- MICA (UNII: V8A1AW0880)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- HEDERA HELIX LEAF (UNII: ZP9XFG71A7)
- FYTIC ACID (UNII: 7IGF0S7R8I)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
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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".