NDC 69750-001 Vertra Elemental Resistance Water Resistant Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 69750-001?
What are the uses for Vertra Elemental Resistance Water Resistant Sunscreen?
Which are Vertra Elemental Resistance Water Resistant Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Vertra Elemental Resistance Water Resistant Sunscreen 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:
- AMMONIA (UNII: 5138Q19F1X)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- LAURYL PEG/PPG-18/18 METHICONE (UNII: ZJ5S27D9NX)
- METHYL GLUCOSE DIOLEATE (UNII: FA9KFJ4Z6P)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- WATER (UNII: 059QF0KO0R)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- XANTHAN GUM (UNII: TTV12P4NEE)
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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".