NDC 71690-201 Aegis Daily Facial Spf 25
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What is NDC 71690-201?
What are the uses for Aegis Daily Facial Spf 25?
Which are Aegis Daily Facial Spf 25 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)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Aegis Daily Facial Spf 25 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:
- ALCOHOL (UNII: 3K9958V90M)
- CARDIOSPERMUM HALICACABUM FLOWERING TOP (UNII: MZP2508BRR)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- ECHIUM PLANTAGINEUM SEED OIL (UNII: PIB7XBU8XW)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
- METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PURSLANE (UNII: M6S840WXG5)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PROPANEDIOL (UNII: 5965N8W85T)
- TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TROMETHAMINE (UNII: 023C2WHX2V)
- WATER (UNII: 059QF0KO0R)
- 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".