NDC 62362-159 Neova Dna Damage Control - Everyday Broad Spectrum Spf 44
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 62362-159?
What are the uses for Neova Dna Damage Control - Everyday Broad Spectrum Spf 44?
Which are Neova Dna Damage Control - Everyday Broad Spectrum Spf 44 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)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Neova Dna Damage Control - Everyday Broad Spectrum Spf 44 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:
- ALLANTOIN (UNII: 344S277G0Z)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ERGOTHIONEINE (UNII: BDZ3DQM98W)
- ETHYLHEXYL ISONONANOATE (UNII: I6KB4GE3K4)
- GLYCERETH-26 (UNII: NNE56F2N14)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- OCTYL STEARATE (UNII: 772Y4UFC8B)
- OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)
- PANTHENOL (UNII: WV9CM0O67Z)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- WATER (UNII: 059QF0KO0R)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
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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".