NDC 69017-101 Anti-blemish Matte Primer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69017 - Jouer Cosmetics Llc
- 69017-101 - Anti-blemish Matte Primer
Product Packages
NDC Code 69017-101-02
Package Description: 1 TUBE in 1 BOX / 30 mL in 1 TUBE (69017-101-01)
NDC Code 69017-101-03
Package Description: 1 mL in 1 PACKET
Product Details
What is NDC 69017-101?
Which are Anti-blemish Matte Primer 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 Matte Primer 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)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STARCH, TAPIOCA (UNII: 24SC3U704I)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- HAMAMELIS VIRGINIANA LEAF WATER (UNII: 8FP93ED6H2)
- OPUNTIA FICUS-INDICA STEM (UNII: MUD8892KHL)
- GINKGO (UNII: 19FUJ2C58T)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
- CARBOMER HOMOPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: F68VH75CJC)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
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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".