NDC 52664-009 Elf Conceler Pencil And Brush
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 52664-009?
What are the uses for Elf Conceler Pencil And Brush?
Which are Elf Conceler Pencil And Brush 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 Elf Conceler Pencil And Brush 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:
- YELLOW WAX (UNII: 2ZA36H0S2V)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- CANDELILLA WAX (UNII: WL0328HX19)
- TEA TREE OIL (UNII: VIF565UC2G)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- MINERAL OIL (UNII: T5L8T28FGP)
- CAMPHOR OIL (UNII: 75IZZ8Y727)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- PETROLATUM (UNII: 4T6H12BN9U)
- MICA (UNII: V8A1AW0880)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- 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 Elf Conceler Pencil And Brush?
- RxCUI: 1047415 - salicylic acid 2 % Paste
- RxCUI: 1047415 - salicylic acid 0.02 MG/MG Paste
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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".