NDC 68479-009 Redness Relief Primer Spf20
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68479 - Dermalogica, Inc.
- 68479-009 - Redness Relief Primer
Product Characteristics
Product Packages
NDC Code 68479-009-00
Package Description: 2 mL in 1 POUCH
NDC Code 68479-009-02
Package Description: 1 TUBE in 1 CARTON / 22 mL in 1 TUBE
Product Details
What is NDC 68479-009?
What are the uses for Redness Relief Primer Spf20?
Which are Redness Relief Primer Spf20 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 Redness Relief Primer Spf20 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:
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ISODODECANE (UNII: A8289P68Y2)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- DIMETHICONE/BIS-ISOBUTYL PPG-20 CROSSPOLYMER (UNII: O4I3UFO6ZF)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- WATER (UNII: 059QF0KO0R)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- OAT KERNEL OIL (UNII: 3UVP41R77R)
- LEVOMENOL (UNII: 24WE03BX2T)
- SACCHAROMYCES LYSATE (UNII: R85W246Z1C)
- GINGER (UNII: C5529G5JPQ)
- BOERHAVIA DIFFUSA ROOT (UNII: KR0SR09KYL)
- AZADIRACHTA INDICA SEED (UNII: P1NV46V59R)
- AZADIRACHTA INDICA LEAF (UNII: HKY915780T)
- OAT (UNII: Z6J799EAJK)
- AMBER (UNII: 70J9Z0J26P)
- COCCINIA GRANDIS FRUIT (UNII: VLJ6WOT3K5)
- EGGPLANT (UNII: W5K7RAS4VK)
- BASIL (UNII: 2U0KZP0FDW)
- CURCUMA LONGA LEAF (UNII: H2HC4RY52C)
- PEARL (HYRIOPSIS CUMINGII) (UNII: A75L5FZ40U)
- DODECENE (UNII: WYE669F3GR)
- HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- POLYETHYLENE GLYCOL 500 (UNII: 761NX2Q08Y)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- 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".