NDC 54111-135 Mario Badescu Spf 17
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 54111-135?
What are the uses for Mario Badescu Spf 17?
Which are Mario Badescu Spf 17 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Mario Badescu Spf 17 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)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- GLYCERIN (UNII: PDC6A3C0OX)
- PPG-2 MYRISTYL ETHER PROPIONATE (UNII: 88R97D8U8A)
- ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PEG-8 LAURATE (UNII: 762O8IWA10)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
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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".