NDC 69863-201 Anti-blemish Concealer
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What is NDC 69863-201?
What are the uses for Anti-blemish Concealer?
Which are Anti-blemish Concealer UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Anti-blemish Concealer 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:
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- STEARYL DIMETHICONE (400 MPA.S AT 50C) (UNII: R327X197HY)
- CANDELILLA WAX (UNII: WL0328HX19)
- CERESIN (UNII: Q1LS2UJO3A)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- ALLYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: B9J55EA6QX)
- TRIDECYL STEARATE (UNII: A8OE252M6L)
- CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- TOCOPHEROL (UNII: R0ZB2556P8)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONOL (2000 CST) (UNII: T74O12AN6Y)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- TRIDECYL TRIMELLITATE (UNII: FY36J270ES)
- NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE (UNII: VLW429K27K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Anti-blemish Concealer?
- RxCUI: 251400 - salicylic acid 2 % Topical Ointment
- RxCUI: 251400 - salicylic acid 0.02 MG/MG Topical Ointment
* Please review the disclaimer below.
[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".