NDC 49527-722 Clinique Redness Solutions Daily Protective Base Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 49527-722?
Which are Clinique Redness Solutions Daily Protective Base Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Clinique Redness Solutions Daily Protective Base Spf 15 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- STEARETH-2 (UNII: V56DFE46J5)
- TRICAPRYLYL CITRATE (UNII: BXW1GAI4TA)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- BARIUM SULFATE (UNII: 25BB7EKE2E)
- SORBITAN TRISTEARATE (UNII: 6LUM696811)
- ALUMINUM STEARATE (UNII: U6XF9NP8HM)
- ASCOPHYLLUM NODOSUM (UNII: 168S4EO8YJ)
- ASPARAGOPSIS ARMATA (UNII: 2936KN6I1G)
- PSEUDOPTEROGORGIA ELISABETHAE (UNII: UDY3H1OUX5)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PEG-100 STEARATE (UNII: YD01N1999R)
- SUCROSE (UNII: C151H8M554)
- PANTETHINE (UNII: 7K81IL792L)
- CAFFEINE (UNII: 3G6A5W338E)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- CETETH-2 (UNII: 7H8VAM7778)
- PEG-40 STEARATE (UNII: ECU18C66Q7)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- STEARETH-20 (UNII: L0Q8IK9E08)
- LEVOMENOL (UNII: 24WE03BX2T)
- MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
- SORBITOL (UNII: 506T60A25R)
- SODIUM STEARATE (UNII: QU7E2XA9TG)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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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".