NDC 75936-235 Everyday Sunscreen Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 75936-235?
What are the uses for Everyday Sunscreen Spf 50?
Which are Everyday Sunscreen Spf 50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
Which are Everyday Sunscreen 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:
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ROSEMARY (UNII: IJ67X351P9)
- HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
- BEHENIC ACID (UNII: H390488X0A)
- CETYL BEHENATE (UNII: WFM51TRO3E)
- ISOSTEARYL ISOSTEARATE (UNII: IV0Z586Z4Y)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- TOCOPHEROL (UNII: R0ZB2556P8)
- PANTHENOL (UNII: WV9CM0O67Z)
- ISODODECANE (UNII: A8289P68Y2)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- WATER (UNII: 059QF0KO0R)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
- ROSEWOOD OIL (UNII: F2522O5L7B)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- OCIMUM BASILICUM FLOWERING TOP (UNII: 7SAB275FP2)
- DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
- ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- ORANGE OIL (UNII: AKN3KSD11B)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- PATCHOULI OIL (UNII: F3IN55X5PO)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ALLANTOIN (UNII: 344S277G0Z)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
- RICE BRAN (UNII: R60QEP13IC)
- LAURYL LACTATE (UNII: G5SU0BFK7O)
- LEMON OIL (UNII: I9GRO824LL)
- PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
- SODIUM TRIPOLYPHOSPHATE ANHYDROUS (UNII: 9SW4PFD2FZ)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
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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".