NDC 43115-101 Nia24 Sun Damage Defense Broad Spectrum 100 Percent Mineral Sunscreen Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43115 - Niadyne Inc
- 43115-101 - Nia24 Sun Damage Defense Broad Spectrum 100 Percent Mineral Sunscreen
Product Packages
NDC Code 43115-101-75
Package Description: 1 TUBE in 1 BOX / 75 mL in 1 TUBE
Product Details
What is NDC 43115-101?
What are the uses for Nia24 Sun Damage Defense Broad Spectrum 100 Percent Mineral Sunscreen Spf 30?
Which are Nia24 Sun Damage Defense Broad Spectrum 100 Percent Mineral Sunscreen Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Nia24 Sun Damage Defense Broad Spectrum 100 Percent Mineral Sunscreen 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- MYRISTYL NICOTINATE (UNII: 8QWM6I035C)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 1.5) (UNII: V2W71V8T0X)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)
- DIMETHICONOL (14000 CST) (UNII: M2HW98ZA4V)
- POLYSILICONE-15 (UNII: F8DRP5BB29)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
- BENZOTRIAZOLYL DODECYL P-CRESOL (UNII: 298PX4M11X)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
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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".