NDC 54754-101 Treat And Tint Skin Perfecting Bb Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 54754-101?
What are the uses for Treat And Tint Skin Perfecting Bb Spf 30?
Which are Treat And Tint Skin Perfecting Bb Spf 30 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)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Treat And Tint Skin Perfecting Bb 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PVP/VA COPOLYMER (UNII: D9C330MD8B)
- OCTYLDECANOL (UNII: 07UG7TSU58)
- QUATERNIUM-18 (UNII: O7757NO1VL)
- HECTORITE (UNII: 08X4KI73EZ)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PENTAERYTHRITYL TETRAETHYLHEXANOATE (UNII: XJ7052W897)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- POLYSILICONE-15 (UNII: F8DRP5BB29)
- CETYL ESTERS WAX (UNII: D072FFP9GU)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- CETEARETH-22 (UNII: 28VZG1E234)
- CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ)
- CARICA PAPAYA WHOLE (UNII: S0U63B0Q51)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ROSMARINUS OFFICINALIS WHOLE (UNII: EA3289138M)
- MATRICARIA CHAMOMILLA WHOLE (UNII: 2Z4LRR776S)
- PANAX GINSENG ROOT WATER (UNII: P9T4K47OM0)
- PASSIFLORA INCARNATA FRUIT (UNII: SF206I8G4P)
- OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
- ARGAN OIL (UNII: 4V59G5UW9X)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- BROWN IRON OXIDE (UNII: 1N032N7MFO)
- MICA (UNII: V8A1AW0880)
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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".