NDC 13537-057 Esika Ultra Softening Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13537 - Ventura Corporation (san Juan, P.r)
- 13537-057 - Esika
Product Characteristics
RED (C48326 - ROJO VIVAZ)
PURPLE (C48327 - FUCSIA FANTASIA)
PURPLE (C48327 - FUCSIA SEDUCTOR)
RED (C48326 - ROSA INTRIGA)
BROWN (C48332 - MORADO OBSESION)
RED (C48326 - ROSA COQUETA)
PINK (C48328 - MALVA ILUSION)
RED (C48326 - VINO SENSUAL)
Product Packages
NDC Code 13537-057-02
Package Description: 1 TUBE in 1 BOX / 4 g in 1 TUBE (13537-057-01)
Product Details
What is NDC 13537-057?
What are the uses for Esika Ultra Softening Spf 15?
Which are Esika Ultra Softening Spf 15 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 Esika Ultra Softening Spf 15 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:
- CASTOR OIL (UNII: D5340Y2I9G)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- CANDELILLA WAX (UNII: WL0328HX19)
- SHEA BUTTER (UNII: K49155WL9Y)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- GLYCERIN (UNII: PDC6A3C0OX)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO)
- ISOSTEARYL ALCOHOL (UNII: Q613OCQ44Y)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- .BETA.-SITOSTEROL (UNII: S347WMO6M4)
- PETROLATUM (UNII: 4T6H12BN9U)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- D&C RED NO. 21 (UNII: 08744Z6JNY)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- MICA (UNII: V8A1AW0880)
- TALC (UNII: 7SEV7J4R1U)
- COCHINEAL (UNII: TZ8Z31B35M)
- ALUMINUM OXIDE (UNII: LMI26O6933)
* Please review the disclaimer below.
[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".