MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15- titanium dioxide and zinc oxide suspension 
Charlotte Tilbury Beauty Ltd.

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Magic Foundation Flawless Long-Lasting Coverage Sunscreen Broad Spectrum SPF 15

Drug Facts

Active Ingredients              Purpose

Titanium Dioxide 3.19%         Sunscreen
Zinc Oxide 0.94%                  Sunscreen

Uses:

• Helps prevent sunburn.

• If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings:

For external use only

Do not useon damaged or broken skin.

When using this productkeep out of eyes. Rinse with water to remove.

Stop use and ask a doctorif rash occurs. water to remove.

Keep out of reach of children.If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions:

• Apply liberally and evenly 15 minutes before sun exposure.
• Children under 6 months of age: Ask a doctor.
Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly     use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 a.m. - 2 p.m.
- wear long-sleeved shirts, pants, hats, and sunglasses.
• Reapply at least every 2 hours or immediately after towel drying.
• Use a water-resistant sunscreen if swimming or sweating.

Inactive Ingredients:

aqua (water), cyclopentasiloxane, cyclohexasiloxane, talc, cetyl peg/ppg-10/1 dimethicone, glycerin, nylon-12, hdi/trimethylol hexyllactone crosspolymer, acrylates/dimethicone copolymer, phenoxyethanol, benzyl alcohol, sodium chloride, magnesium sulfate, hydrogen dimethicone, sodium dehydroacetate, alumina, disteardimonium hectorite, dehydroacetic acid, potassium sorbate, benzoic acid, dimethicone, tetrasodium edta, tocopheryl acetate, aluminum hydroxide, triethoxycaprylylsilane, ascorbyl tetraisopalmitate, propylene carbonate, sodium hyaluronate, butylene glycol, silica, ethylhexylglycerin, fomes officinalis (mushroom) extract), peg-40 hydrogenated castor oil, [may contain/peut contenir (+/-): titanium dioxide (CI 77891), (iron oxides CI 77491, CI 77492, CI 77499).

Other Information:

Protect the product in this container from excessive heat and direct sun.

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Packaging

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MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15 
titanium dioxide and zinc oxide suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70186-566
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.957 g  in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.282 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
TALC (UNII: 7SEV7J4R1U)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
NYLON-12 (UNII: 446U8J075B)  
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
EDETATE SODIUM (UNII: MP1J8420LU)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Product Characteristics
Colorbrown (1 Fair) Score    
ShapeCAPSULESize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70186-566-011 in 1 CARTON02/22/201610/31/2018
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02002/22/201610/31/2018
MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15 
titanium dioxide and zinc oxide suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70186-567
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.957 g  in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.282 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
TALC (UNII: 7SEV7J4R1U)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
NYLON-12 (UNII: 446U8J075B)  
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
EDETATE SODIUM (UNII: MP1J8420LU)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Product Characteristics
Colorbrown (2 Fair) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70186-567-011 in 1 CARTON02/22/201610/31/2018
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02002/22/201610/31/2018
MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15 
titanium dioxide and zinc oxide suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70186-568
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.957 g  in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.282 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
TALC (UNII: 7SEV7J4R1U)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
NYLON-12 (UNII: 446U8J075B)  
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
EDETATE SODIUM (UNII: MP1J8420LU)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Product Characteristics
Colorbrown (3 Fair) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70186-568-011 in 1 CARTON02/22/201610/31/2018
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02002/22/201610/31/2018
MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15 
titanium dioxide and zinc oxide suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70186-569
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.957 g  in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.282 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
TALC (UNII: 7SEV7J4R1U)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
NYLON-12 (UNII: 446U8J075B)  
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
EDETATE SODIUM (UNII: MP1J8420LU)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Product Characteristics
Colorbrown (3.5 Fair) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70186-569-011 in 1 CARTON02/22/201610/31/2018
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02002/22/201610/31/2018
MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15 
titanium dioxide and zinc oxide suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70186-570
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.957 g  in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.282 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
TALC (UNII: 7SEV7J4R1U)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
NYLON-12 (UNII: 446U8J075B)  
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
EDETATE SODIUM (UNII: MP1J8420LU)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Product Characteristics
Colorbrown (4 Fair) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70186-570-011 in 1 CARTON02/22/201610/31/2018
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02002/22/201610/31/2018
MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15 
titanium dioxide and zinc oxide suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70186-571
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.957 g  in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.282 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
TALC (UNII: 7SEV7J4R1U)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
NYLON-12 (UNII: 446U8J075B)  
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
EDETATE SODIUM (UNII: MP1J8420LU)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Product Characteristics
Colorbrown (4.5 Medium) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70186-571-011 in 1 CARTON02/22/201610/31/2018
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02002/22/201610/31/2018
MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15 
titanium dioxide and zinc oxide suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70186-572
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.957 g  in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.282 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
NYLON-12 (UNII: 446U8J075B)  
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
TALC (UNII: 7SEV7J4R1U)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
EDETATE SODIUM (UNII: MP1J8420LU)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Product Characteristics
Colorbrown (5 Medium) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70186-572-011 in 1 CARTON02/22/201605/31/2018
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02002/22/201605/31/2018
MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15 
titanium dioxide and zinc oxide suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70186-573
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.957 g  in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.282 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
TALC (UNII: 7SEV7J4R1U)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
NYLON-12 (UNII: 446U8J075B)  
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
EDETATE SODIUM (UNII: MP1J8420LU)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Product Characteristics
Colorbrown (6 Medium) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70186-573-011 in 1 CARTON02/22/201610/31/2018
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02002/22/201610/31/2018
MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15 
titanium dioxide and zinc oxide suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70186-574
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.957 g  in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.282 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
TALC (UNII: 7SEV7J4R1U)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
NYLON-12 (UNII: 446U8J075B)  
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
EDETATE SODIUM (UNII: MP1J8420LU)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Product Characteristics
Colorbrown (7 Medium) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70186-574-011 in 1 CARTON02/22/201605/31/2018
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02002/22/201605/31/2018
MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15 
titanium dioxide and zinc oxide suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70186-575
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.957 g  in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.282 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
TALC (UNII: 7SEV7J4R1U)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
NYLON-12 (UNII: 446U8J075B)  
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
EDETATE SODIUM (UNII: MP1J8420LU)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Product Characteristics
Colorbrown (8 Medium) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70186-575-011 in 1 CARTON02/22/201610/31/2018
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02002/22/201610/31/2018
MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15 
titanium dioxide and zinc oxide suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70186-576
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.957 g  in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.282 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
TALC (UNII: 7SEV7J4R1U)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
NYLON-12 (UNII: 446U8J075B)  
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
EDETATE SODIUM (UNII: MP1J8420LU)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Product Characteristics
Colorbrown (9 Dark) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70186-576-011 in 1 CARTON02/22/201607/31/2017
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02002/22/201607/31/2017
MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15 
titanium dioxide and zinc oxide suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70186-577
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.957 g  in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.282 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
TALC (UNII: 7SEV7J4R1U)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
NYLON-12 (UNII: 446U8J075B)  
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
EDETATE SODIUM (UNII: MP1J8420LU)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Product Characteristics
Colorbrown (9.5 Dark) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70186-577-011 in 1 CARTON02/22/201611/30/2018
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02002/22/201611/30/2018
MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15 
titanium dioxide and zinc oxide suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70186-579
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.957 g  in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.282 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
TALC (UNII: 7SEV7J4R1U)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
NYLON-12 (UNII: 446U8J075B)  
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
EDETATE SODIUM (UNII: MP1J8420LU)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Product Characteristics
Colorbrown (10 Dark) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70186-579-011 in 1 CARTON02/22/201610/31/2018
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02002/22/201610/31/2018
MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15 
titanium dioxide and zinc oxide suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70186-578
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.957 g  in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.282 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
TALC (UNII: 7SEV7J4R1U)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
NYLON-12 (UNII: 446U8J075B)  
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
EDETATE SODIUM (UNII: MP1J8420LU)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Product Characteristics
Colorbrown (11 Dark) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70186-578-011 in 1 CARTON02/22/201610/31/2018
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02002/22/201610/31/2018
MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15 
titanium dioxide and zinc oxide suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70186-564
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.957 g  in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.282 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
TALC (UNII: 7SEV7J4R1U)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
NYLON-12 (UNII: 446U8J075B)  
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
EDETATE SODIUM (UNII: MP1J8420LU)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Product Characteristics
Colorbrown (12 Dark) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70186-564-011 in 1 CARTON02/22/201610/31/2018
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02002/22/201610/31/2018
Labeler - Charlotte Tilbury Beauty Ltd. (218353520)

Revised: 2/2025
 
Charlotte Tilbury Beauty Ltd.