NDC 11559-732 Double Matte Oil Control Makeup Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 11559-732?
Which are Double Matte Oil Control Makeup Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Double Matte Oil Control Makeup Spf 15 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- COCONUT ACID (UNII: 40U37V505D)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- URTICA DIOICA LEAF (UNII: X6M0DRN46Q)
- MELISSA OFFICINALIS (UNII: YF70189L0N)
- EQUISETUM HYEMALE (UNII: 59677RXH25)
- AESCULUS HIPPOCASTANUM BARK (UNII: 7U76MXL14N)
- ROSEMARY (UNII: IJ67X351P9)
- SAGE (UNII: 065C5D077J)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- KAOLIN (UNII: 24H4NWX5CO)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- LAURETH-7 (UNII: Z95S6G8201)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- 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".