NDC 82038-002 Protectif Deep Tint
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 82038-002?
What are the uses for Protectif Deep Tint?
Which are Protectif Deep Tint 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)
Which are Protectif Deep Tint 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:
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- APPLE (UNII: B423VGH5S9)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CYCLOTETRAPEPTIDE-24 AMINOCYCLOHEXANE CARBOXYLATE (UNII: NR327745KQ)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 4) (UNII: 8INO2K35FA)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- ALCOHOL (UNII: 3K9958V90M)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- ISOMALT (UNII: S870P55O2W)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- ARABICA COFFEE BEAN (UNII: 3SW678MX72)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CYCLOMETHICONE 4 (UNII: CZ227117JE)
- HYDROXYTYROSOL (UNII: QEU0NE4O90)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- SODIUM FERROCYANIDE DECAHYDRATE (UNII: CG0CLR485X)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- ECTOINE (UNII: 7GXZ3858RY)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- DIMETHICONE/POLYGLYCERIN-3 CROSSPOLYMER (UNII: 2P2G24V6T9)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- POLYGONUM AVICULARE TOP (UNII: ZCD6009IUF)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- VITIS VINIFERA STEM (UNII: K1Z31TDY7Z)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- WATER (UNII: 059QF0KO0R)
- POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)
- TOCOPHEROL (UNII: R0ZB2556P8)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TRIETHOXYSILYLETHYL POLYDIMETHYLSILOXYETHYL HEXYL DIMETHICONE (UNII: X75PL53TZJ)
- PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
* 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".