NDC 13537-661 Esika Pro Multi-gloss Dual With Triple Gloss Effect Spf 15 (diamante Rosa) - Pink
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What is NDC 13537-661?
What are the uses for Esika Pro Multi-gloss Dual With Triple Gloss Effect Spf 15 (diamante Rosa) - Pink?
Which are Esika Pro Multi-gloss Dual With Triple Gloss Effect Spf 15 (diamante Rosa) - Pink UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Esika Pro Multi-gloss Dual With Triple Gloss Effect Spf 15 (diamante Rosa) - 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:
- DIISOPROPYL DILINOLEATE (UNII: 5323S7S2LR)
- DIPENTAERYTHRITYL HEXACAPRYLATE/HEXACAPRATE (UNII: 554N82UWVW)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- TRIDECYL TRIMELLITATE (UNII: FY36J270ES)
- CANDELILLA WAX (UNII: WL0328HX19)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- SHEA BUTTER (UNII: K49155WL9Y)
- TRIDECYL STEARATE (UNII: A8OE252M6L)
- NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE (UNII: VLW429K27K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO)
- ISOSTEARYL ALCOHOL (UNII: Q613OCQ44Y)
- .BETA.-SITOSTEROL (UNII: S347WMO6M4)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CERAMIDE 3 (UNII: 4370DF050B)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- PARAFFIN (UNII: I9O0E3H2ZE)
- D&C RED NO. 21 (UNII: 08744Z6JNY)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- MICA (UNII: V8A1AW0880)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- TALC (UNII: 7SEV7J4R1U)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
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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".