NDC 75936-215 Everyday Sunscreen Spf 50 With Sunflower Extract
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 75936-215?
What are the uses for Everyday Sunscreen Spf 50 With Sunflower Extract?
Which are Everyday Sunscreen Spf 50 With Sunflower Extract UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
Which are Everyday Sunscreen Spf 50 With Sunflower Extract 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ALLANTOIN (UNII: 344S277G0Z)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- PANTHENOL (UNII: WV9CM0O67Z)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- RICE BRAN (UNII: R60QEP13IC)
- ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)
- LAURYL LACTATE (UNII: G5SU0BFK7O)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETYL BEHENATE (UNII: WFM51TRO3E)
- ISOSTEARYL ISOSTEARATE (UNII: IV0Z586Z4Y)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
- TOCOPHEROL (UNII: R0ZB2556P8)
- SODIUM TRIPOLYPHOSPHATE ANHYDROUS (UNII: 9SW4PFD2FZ)
- LEMON OIL (UNII: I9GRO824LL)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ROSEMARY (UNII: IJ67X351P9)
- ISODODECANE (UNII: A8289P68Y2)
- POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- ROSEWOOD OIL (UNII: F2522O5L7B)
- ORANGE OIL (UNII: AKN3KSD11B)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PATCHOULI OIL (UNII: F3IN55X5PO)
- BEHENIC ACID (UNII: H390488X0A)
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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".