NDC 13537-165 Lbel Couleur Luxe Rouge Amplifier Xp Amplifying Spf 15 (fiancee) - Pink
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Product Details
What is NDC 13537-165?
What are the uses for Lbel Couleur Luxe Rouge Amplifier Xp Amplifying Spf 15 (fiancee) - Pink?
Which are Lbel Couleur Luxe Rouge Amplifier Xp Amplifying Spf 15 (fiancee) - Pink UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Lbel Couleur Luxe Rouge Amplifier Xp Amplifying Spf 15 (fiancee) - Pink 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:
- ISOSTEARYL NEOPENTANOATE (UNII: 411THY156Q)
- DIISOPROPYL DILINOLEATE (UNII: 5323S7S2LR)
- MICA (UNII: V8A1AW0880)
- METHYL HYDROGENATED ROSINATE (UNII: 13DHA19W9N)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- CANDELILLA WAX (UNII: WL0328HX19)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- ISODODECANE (UNII: A8289P68Y2)
- PARAFFIN (UNII: I9O0E3H2ZE)
- POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
- GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO)
- ISOSTEARYL ALCOHOL (UNII: Q613OCQ44Y)
- DIPALMITOYL HYDROXYPROLINE (UNII: E6AHA53N1H)
- CERAMIDE 3 (UNII: 4370DF050B)
- SHEA BUTTER (UNII: K49155WL9Y)
- .BETA.-SITOSTEROL (UNII: S347WMO6M4)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- LUFFA AEGYPTIACA SEED OIL (UNII: 1A281RJ859)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PPG-26-BUTETH-26 (UNII: 2II1K6TZ4P)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- HEDERA HELIX LEAF (UNII: ZP9XFG71A7)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALLANTOIN (UNII: 344S277G0Z)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- MANGANESE VIOLET (UNII: 72M48QQV8Q)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- D&C RED NO. 21 (UNII: 08744Z6JNY)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- D&C RED NO. 6 (UNII: 481744AI4O)
- TALC (UNII: 7SEV7J4R1U)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- LAUROYL LYSINE (UNII: 113171Q70B)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".