NDC 20151-096 Shine Control Matte Effect Cream
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 20151-096?
What are the uses for Shine Control Matte Effect Cream?
Which are Shine Control Matte Effect Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Shine Control Matte Effect Cream 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:
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- WATER (UNII: 059QF0KO0R)
- CETYL ACETATE (UNII: 4Q43814HXS)
- EGG YOLK (UNII: 4IPS17B70T)
- METHYLPROPANEDIOL (UNII: N8F53B3R4R)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- XANTHAN GUM (UNII: TTV12P4NEE)
- JOJOBA OIL (UNII: 724GKU717M)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
- PERFLUNAFENE (UNII: 54A06VV62N)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- HYDROLYZED JOJOBA ESTERS (POTASSIUM SALTS) (UNII: CH428W5O62)
- CETYL PHOSPHATE (UNII: VT07D6X67O)
- POTASSIUM AZELOYL DIGLYCINATE (UNII: N02RVN6NYP)
- CERAMIDE NP (UNII: 4370DF050B)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SILANETRIOL (UNII: E52D0J3TS5)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- SUCROSE PALMITATE (UNII: 3OSQ643ZK5)
- RHAMNOSE (UNII: QN34XC755A)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
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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".