NDC 66854-026 Dermaprot Helioprot Ab Spf 30
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What is NDC 66854-026?
What are the uses for Dermaprot Helioprot Ab Spf 30?
Which are Dermaprot Helioprot Ab Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Dermaprot Helioprot Ab 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CHAMOMILE (UNII: FGL3685T2X)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)
- CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
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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".