NDC 72284-0003 Im Cover Bb Sunstick
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 72284-0003?
Which are Im Cover Bb Sunstick UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Im Cover Bb Sunstick 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:
- CONVALLARIA MAJALIS (UNII: QHH4HVF5QE)
- CAMELLIA JAPONICA FLOWER (UNII: KUB8101TNF)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- NYLON-12 (UNII: 446U8J075B)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- SUCROSE TETRASTEARATE TRIACETATE (UNII: 1K7LBQ045N)
- STEARALKONIUM HECTORITE (UNII: OLX698AH5P)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- TROPOLONE (UNII: 7L6DL16P1T)
- CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- METHYL HYDROGENATED ROSINATE (UNII: 13DHA19W9N)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- SQUALANE (UNII: GW89575KF9)
- IPOMOEA PURPUREA TOP (UNII: XMQ0V9812O)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- WATER (UNII: 059QF0KO0R)
- MICA (UNII: V8A1AW0880)
- RICINUS COMMUNIS SEED (UNII: 7EK4SFN1TX)
- METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: 657L0NC5MT)
- WHITE WAX (UNII: 7G1J5DA97F)
- BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI)
- CANDELILLA WAX (UNII: WL0328HX19)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- GLYCERIN (UNII: PDC6A3C0OX)
- MACADAMIA OIL (UNII: 515610SU8C)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)
- LILIUM CANDIDUM FLOWER (UNII: COV655U2CJ)
- MAGNOLIA LILIIFLORA FLOWER (UNII: SVM28292LH)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CHAMOMILE (UNII: FGL3685T2X)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CERAMIDE NP (UNII: 4370DF050B)
* 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".