NDC 70528-018 Zrii New Day Broad Spectrum Spf-30
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 70528-018?
What are the uses for Zrii New Day Broad Spectrum Spf-30?
Which are Zrii New Day Broad Spectrum Spf-30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Zrii New Day Broad Spectrum Spf-30 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)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)
- CETEARETH-22 (UNII: 28VZG1E234)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- NIACINAMIDE (UNII: 25X51I8RD4)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- PSEUDOPTEROGORGIA ELISABETHAE (UNII: UDY3H1OUX5)
- DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
- LAURYL LACTATE (UNII: G5SU0BFK7O)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- 7-DEHYDROCHOLESTEROL (UNII: BK1IU07GKF)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
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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".