DailyMed - MATCH PERFECTION FOUNDATION SPF 20 - SHADE 100 IVORY- octinoxate and titanium dioxide liquid MATCH PERFECTION FOUNDATION SPF 20 - SHADE 300 SAND- octinoxate and titanium dioxide liquid MATCH PERFECTION FOUNDATION SPF 20 - SHADE 301 WARM HONEY- octinoxate and titanium dioxide liquid MATCH PERFECTION FOUNDATION SPF 20 - SHADE 302 GOLDEN HONEY- octinoxate and titanium dioxide liquid MATCH PERFECTION FOUNDATION SPF 20 - SHADE 303 TRUE NUDE- octinoxate and titanium dioxide liquid MATCH PERFECTION FOUNDATION SPF 20 - SHADE 400 NATURAL BEIGE- octinoxate and titanium dioxide liquid MATCH PERFECTION FOUNDATION SPF 20 - SHADE 101 CLASSIC IVORY- octinoxate and titanium dioxide liquid MATCH PERFECTION FOUNDATION SPF 20 - SHADE 102 LIGHT NUDE- octinoxate and titanium dioxide liquid MATCH PERFECTION FOUNDATION SPF 20 - SHADE 103 TRUE IVORY- octinoxate and titanium dioxide liquid MATCH PERFECTION FOUNDATION SPF 20 - SHADE 200 BEIGE- octinoxate and titanium dioxide liquid MATCH PERFECTION FOUNDATION SPF 20 - SHADE 402 BRONZE- octinoxate and titanium dioxide liquid MATCH PERFECTION FOUNDATION SPF 20 - SHADE 201 CLASSIC BEIGE- octinoxate and titanium dioxide liquid MATCH PERFECTION FOUNDATION SPF 20 - SHADE 202 NUDE- octinoxate and titanium dioxide liquid MATCH PERFECTION FOUNDATION SPF 20 - SHADE 203 TRUE BEIGE- octinoxate and titanium dioxide liquid

Contains inactivated NDC Code(s)
NDC Code(s): 76485-1050-1, 76485-1051-1, 76485-1052-1, 76485-1053-1, view more
76485-1054-1, 76485-1054-2, 76485-1055-1, 76485-1056-1, 76485-1057-1, 76485-1058-1, 76485-1059-1, 76485-1060-1, 76485-1061-1, 76485-1062-1, 76485-1063-1
Packager: Rimmel Inc.

Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated October 26, 2020

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

Download DRUG LABEL INFO: PDF XML
Official Label (Printer Friendly)

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SPL UNCLASSIFIED SECTION

Drug Facts
Active ingredients

Octinoxate 4%

Titanium Dioxide 7.43%
Purpose

Sunscreen

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 use on damaged or broken skin.

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

Stop use and ask a doctor if rash occurs.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
For sunscreen use:
- apply liberally 15 minutes before sun exposure
- reapply at least every 2 hours
- use a water resistant sunscreen if swimming or sweating
- 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 value of 15 SPF 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 • Children under 6 months of age: ask a doctor
Other information

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

aqua/water/eau, cyclopentasiloxane, dicaprylyl ether, talc, cetyl peg/ppg-10/1 dimethicone, glycerin, propylene glycol, peg-10 dimethicone, quaternium-90 sepiolite, dimethicone/vinyl dimethicone crosspolymer, acrylates crosspolymer, sodium chloride, lecithin, mica, trihydroxystearin, aluminum starch octenylsuccinate, quaternium-90 montmorillonite, ammonium acrylates copolymer, chlorphenesin, phenoxyethanol, tribehenin, parfum/fragrance, disodium stearoyl glutamate, alcohol denat., disodium edta, disodium deceth-6 sulfosuccinate, aluminum hydroxide, laureth-4, hexyl cinnamal, laureth-30, limonene, tocopheryl acetate, butylphenyl methylpropional, benzyl salicylate, linalool, geraniol, bht, sodium dehydroacetate, citronellol, alpha-isomethyl ionone, pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate, [may contain/peut contenir/+/-: iron oxides (ci 77491, ci 77492, ci 77499)].
Questions or comments?

Call 1- 800- 715-4023 9:00 am to 5:00 pm ET Monday - Friday
Principal Display Panel - Bottle Label

RIMMEL

LONDON

MATCH
PERFECTION

24HR
MOISTURE

PORE
BLURRING
EFFECT

BROAD
SPECTRUM
SPF 20

SUNSCREEN FOUNDATION

INVISIBLE COVERAGE

VISIBLY PERFECTED SKIN

100 (120) IVORY

1 fl oz 30 ml
Principal Display Panel - Bottle Label

RIMMEL

LONDON

MATCH
PERFECTION

24HR
MOISTURE

PORE
BLURRING
EFFECT

BROAD
SPECTRUM
SPF 20

SUNSCREEN FOUNDATION

INVISIBLE COVERAGE

VISIBLY PERFECTED SKIN

101 CLASSIC IVORY

1 fl oz 30 ml
Principal Display Panel - Bottle Label

RIMMEL

LONDON

MATCH
PERFECTION

24HR
MOISTURE

PORE
BLURRING
EFFECT

BROAD
SPECTRUM
SPF 20

SUNSCREEN FOUNDATION

INVISIBLE COVERAGE

VISIBLY PERFECTED SKIN

102 LIGHT NUDE

1 fl oz 30 ml
Principal Display Panel - Bottle Label

RIMMEL

LONDON

MATCH
PERFECTION

24HR
MOISTURE

PORE
BLURRING
EFFECT

BROAD
SPECTRUM
SPF 20

SUNSCREEN FOUNDATION

INVISIBLE COVERAGE

VISIBLY PERFECTED SKIN

103 (130) TRUE IVORY

1 fl oz 30 ml
Principal Display Panel - Bottle Label

RIMMEL

LONDON

MATCH
PERFECTION

24HR
MOISTURE

PORE
BLURRING
EFFECT

BROAD
SPECTRUM
SPF 20

SUNSCREEN FOUNDATION

INVISIBLE COVERAGE

VISIBLY PERFECTED SKIN

200 (240) SOFT BEIGE

1 fl oz 30 ml
Principal Display Panel - Bottle Label

RIMMEL

LONDON

MATCH
PERFECTION

24 HR
MOISTURE

PORE
BLURRING
EFFECT

SUNSCREEN FOUNDATION

INVISIBLE COVERAGE

VISIBLY PERFECTED SKIN

BROAD SPECTRUM
SPF 20

200 (240) SOFT BEIGE

0.05 fl oz / 1.5 ml
Principal Display Panel - Bottle Label

RIMMEL

LONDON

MATCH
PERFECTION

24HR
MOISTURE

PORE
BLURRING
EFFECT

BROAD
SPECTRUM
SPF 20

SUNSCREEN FOUNDATION

INVISIBLE COVERAGE

VISIBLY PERFECTED SKIN

402 BRONZE

1 fl oz 30 ml
Principal Display Panel - Bottle Label

RIMMEL

LONDON

MATCH
PERFECTION

24HR
MOISTURE

PORE
BLURRING
EFFECT

BROAD
SPECTRUM
SPF 20

SUNSCREEN FOUNDATION

INVISIBLE COVERAGE

VISIBLY PERFECTED SKIN

201(250) CLASSIC BEIGE

1 fl oz 30 ml
Principal Display Panel - Bottle Label

RIMMEL

LONDON

MATCH
PERFECTION

24HR
MOISTURE

PORE
BLURRING
EFFECT

BROAD
SPECTRUM
SPF 20

SUNSCREEN FOUNDATION

INVISIBLE COVERAGE

VISIBLY PERFECTED SKIN

203 TRUE BEIGE

1 fl oz 30 ml
Principal Display Panel - Bottle Label

RIMMEL

LONDON

MATCH
PERFECTION

24HR
MOISTURE

PORE
BLURRING
EFFECT

BROAD
SPECTRUM
SPF 20

SUNSCREEN FOUNDATION

INVISIBLE COVERAGE

VISIBLY PERFECTED SKIN

300(330) SAND

1 fl oz 30 ml
Principal Display Panel - Bottle Label

RIMMEL

LONDON

MATCH
PERFECTION

24HR
MOISTURE

PORE
BLURRING
EFFECT

BROAD
SPECTRUM
SPF 20

SUNSCREEN FOUNDATION

INVISIBLE COVERAGE

VISIBLY PERFECTED SKIN

301 WARM HONEY

1 fl oz 30 ml
Principal Display Panel - Bottle Label

RIMMEL

LONDON

MATCH
PERFECTION

24HR
MOISTURE

PORE
BLURRING
EFFECT

BROAD
SPECTRUM
SPF 20

SUNSCREEN FOUNDATION

INVISIBLE COVERAGE

VISIBLY PERFECTED SKIN

302 GOLDEN HONEY

1 fl oz 30 ml
Principal Display Panel - Bottle Label

RIMMEL

LONDON

MATCH
PERFECTION

24HR
MOISTURE

PORE
BLURRING
EFFECT

BROAD
SPECTRUM
SPF 20

SUNSCREEN FOUNDATION

INVISIBLE COVERAGE

VISIBLY PERFECTED SKIN

303 TRUE NUDE

1 fl oz 30 ml
Principal Display Panel - Bottle Label

RIMMEL

LONDON

MATCH
PERFECTION

24HR
MOISTURE

PORE
BLURRING
EFFECT

BROAD
SPECTRUM
SPF 20

SUNSCREEN FOUNDATION

INVISIBLE COVERAGE

VISIBLY PERFECTED SKIN

400 NATURAL BEIGE

1 fl oz 30 ml

INGREDIENTS AND APPEARANCE

MATCH PERFECTION FOUNDATION SPF 20 - SHADE 100 IVORY
octinoxate and titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76485-1050
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.278 g in 30 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.374 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
TALC (UNII: 7SEV7J4R1U)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
QUATERNIUM-91 (UNII: 00J8H295NB)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
MICA (UNII: V8A1AW0880)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
MONTMORILLONITE (UNII: A585MN1H2L)
AMMONIA (UNII: 5138Q19F1X)
CHLORPHENESIN (UNII: I670DAL4SZ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
ALCOHOL (UNII: 3K9958V90M)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DECETH-6 (UNII: P4OYN7A2O9)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
LAURETH-4 (UNII: 6HQ855798J)
LAURETH-30 (UNII: W9D845551A)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:76485-1050-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	01/01/2016	10/01/2020

MATCH PERFECTION FOUNDATION SPF 20 - SHADE 300 SAND
octinoxate and titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76485-1058
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.278 g in 30 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.374 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
MICA (UNII: V8A1AW0880)
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
TALC (UNII: 7SEV7J4R1U)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
QUATERNIUM-91 (UNII: 00J8H295NB)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
MONTMORILLONITE (UNII: A585MN1H2L)
AMMONIA (UNII: 5138Q19F1X)
CHLORPHENESIN (UNII: I670DAL4SZ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
ALCOHOL (UNII: 3K9958V90M)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DECETH-6 (UNII: P4OYN7A2O9)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
LAURETH-4 (UNII: 6HQ855798J)
LAURETH-30 (UNII: W9D845551A)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:76485-1058-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	01/01/2016	10/01/2020

MATCH PERFECTION FOUNDATION SPF 20 - SHADE 301 WARM HONEY
octinoxate and titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76485-1059
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.278 g in 30 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.374 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
EDETATE DISODIUM (UNII: 7FLD91C86K)
DECETH-6 (UNII: P4OYN7A2O9)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
LAURETH-4 (UNII: 6HQ855798J)
LAURETH-30 (UNII: W9D845551A)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
TALC (UNII: 7SEV7J4R1U)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
QUATERNIUM-91 (UNII: 00J8H295NB)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
MICA (UNII: V8A1AW0880)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
MONTMORILLONITE (UNII: A585MN1H2L)
AMMONIA (UNII: 5138Q19F1X)
CHLORPHENESIN (UNII: I670DAL4SZ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
ALCOHOL (UNII: 3K9958V90M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:76485-1059-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	01/01/2016	10/01/2020

MATCH PERFECTION FOUNDATION SPF 20 - SHADE 302 GOLDEN HONEY
octinoxate and titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76485-1060
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.278 g in 30 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.374 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
TALC (UNII: 7SEV7J4R1U)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
QUATERNIUM-91 (UNII: 00J8H295NB)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
MICA (UNII: V8A1AW0880)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
MONTMORILLONITE (UNII: A585MN1H2L)
AMMONIA (UNII: 5138Q19F1X)
CHLORPHENESIN (UNII: I670DAL4SZ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
ALCOHOL (UNII: 3K9958V90M)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DECETH-6 (UNII: P4OYN7A2O9)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
LAURETH-4 (UNII: 6HQ855798J)
LAURETH-30 (UNII: W9D845551A)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:76485-1060-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	01/01/2016	10/01/2020

MATCH PERFECTION FOUNDATION SPF 20 - SHADE 303 TRUE NUDE
octinoxate and titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76485-1061
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.278 g in 30 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.374 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
TALC (UNII: 7SEV7J4R1U)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
QUATERNIUM-91 (UNII: 00J8H295NB)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
MICA (UNII: V8A1AW0880)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
MONTMORILLONITE (UNII: A585MN1H2L)
AMMONIA (UNII: 5138Q19F1X)
CHLORPHENESIN (UNII: I670DAL4SZ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
ALCOHOL (UNII: 3K9958V90M)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DECETH-6 (UNII: P4OYN7A2O9)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
LAURETH-4 (UNII: 6HQ855798J)
LAURETH-30 (UNII: W9D845551A)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:76485-1061-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	01/01/2016	10/01/2020

MATCH PERFECTION FOUNDATION SPF 20 - SHADE 400 NATURAL BEIGE
octinoxate and titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76485-1062
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.278 g in 30 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.374 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
TALC (UNII: 7SEV7J4R1U)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
QUATERNIUM-91 (UNII: 00J8H295NB)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
MICA (UNII: V8A1AW0880)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
MONTMORILLONITE (UNII: A585MN1H2L)
AMMONIA (UNII: 5138Q19F1X)
CHLORPHENESIN (UNII: I670DAL4SZ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
ALCOHOL (UNII: 3K9958V90M)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DECETH-6 (UNII: P4OYN7A2O9)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
LAURETH-4 (UNII: 6HQ855798J)
LAURETH-30 (UNII: W9D845551A)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:76485-1062-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	01/01/2016	10/01/2020

MATCH PERFECTION FOUNDATION SPF 20 - SHADE 101 CLASSIC IVORY
octinoxate and titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76485-1051
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.278 g in 30 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.374 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
TALC (UNII: 7SEV7J4R1U)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
QUATERNIUM-91 (UNII: 00J8H295NB)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
MICA (UNII: V8A1AW0880)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
MONTMORILLONITE (UNII: A585MN1H2L)
AMMONIA (UNII: 5138Q19F1X)
CHLORPHENESIN (UNII: I670DAL4SZ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
ALCOHOL (UNII: 3K9958V90M)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DECETH-6 (UNII: P4OYN7A2O9)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
LAURETH-4 (UNII: 6HQ855798J)
LAURETH-30 (UNII: W9D845551A)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:76485-1051-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	01/01/2016

MATCH PERFECTION FOUNDATION SPF 20 - SHADE 102 LIGHT NUDE
octinoxate and titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76485-1052
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.278 g in 30 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.374 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
TALC (UNII: 7SEV7J4R1U)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
QUATERNIUM-91 (UNII: 00J8H295NB)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
MICA (UNII: V8A1AW0880)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
MONTMORILLONITE (UNII: A585MN1H2L)
AMMONIA (UNII: 5138Q19F1X)
CHLORPHENESIN (UNII: I670DAL4SZ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
ALCOHOL (UNII: 3K9958V90M)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DECETH-6 (UNII: P4OYN7A2O9)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
LAURETH-4 (UNII: 6HQ855798J)
LAURETH-30 (UNII: W9D845551A)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:76485-1052-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	01/01/2016	10/01/2020

MATCH PERFECTION FOUNDATION SPF 20 - SHADE 103 TRUE IVORY
octinoxate and titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76485-1053
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.278 g in 30 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.374 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
TALC (UNII: 7SEV7J4R1U)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
QUATERNIUM-91 (UNII: 00J8H295NB)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
MICA (UNII: V8A1AW0880)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
MONTMORILLONITE (UNII: A585MN1H2L)
AMMONIA (UNII: 5138Q19F1X)
CHLORPHENESIN (UNII: I670DAL4SZ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
ALCOHOL (UNII: 3K9958V90M)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DECETH-6 (UNII: P4OYN7A2O9)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
LAURETH-4 (UNII: 6HQ855798J)
LAURETH-30 (UNII: W9D845551A)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:76485-1053-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	01/01/2016	10/01/2020

MATCH PERFECTION FOUNDATION SPF 20 - SHADE 200 BEIGE
octinoxate and titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76485-1054
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.278 g in 30 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.374 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
TALC (UNII: 7SEV7J4R1U)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
QUATERNIUM-91 (UNII: 00J8H295NB)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
MICA (UNII: V8A1AW0880)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
MONTMORILLONITE (UNII: A585MN1H2L)
AMMONIA (UNII: 5138Q19F1X)
CHLORPHENESIN (UNII: I670DAL4SZ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
ALCOHOL (UNII: 3K9958V90M)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DECETH-6 (UNII: P4OYN7A2O9)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
LAURETH-4 (UNII: 6HQ855798J)
LAURETH-30 (UNII: W9D845551A)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:76485-1054-1	1.5 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016
2	NDC:76485-1054-2	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	01/01/2016	10/01/2020

MATCH PERFECTION FOUNDATION SPF 20 - SHADE 402 BRONZE
octinoxate and titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76485-1063
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.278 g in 30 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.374 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
TALC (UNII: 7SEV7J4R1U)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
QUATERNIUM-91 (UNII: 00J8H295NB)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
MICA (UNII: V8A1AW0880)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
MONTMORILLONITE (UNII: A585MN1H2L)
AMMONIA (UNII: 5138Q19F1X)
CHLORPHENESIN (UNII: I670DAL4SZ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
ALCOHOL (UNII: 3K9958V90M)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DECETH-6 (UNII: P4OYN7A2O9)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
LAURETH-4 (UNII: 6HQ855798J)
LAURETH-30 (UNII: W9D845551A)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:76485-1063-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	01/01/2016	10/01/2020

MATCH PERFECTION FOUNDATION SPF 20 - SHADE 201 CLASSIC BEIGE
octinoxate and titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76485-1055
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.278 g in 30 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.374 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
TALC (UNII: 7SEV7J4R1U)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
QUATERNIUM-91 (UNII: 00J8H295NB)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
MICA (UNII: V8A1AW0880)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
MONTMORILLONITE (UNII: A585MN1H2L)
AMMONIA (UNII: 5138Q19F1X)
CHLORPHENESIN (UNII: I670DAL4SZ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
ALCOHOL (UNII: 3K9958V90M)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DECETH-6 (UNII: P4OYN7A2O9)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
LAURETH-4 (UNII: 6HQ855798J)
LAURETH-30 (UNII: W9D845551A)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:76485-1055-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	01/01/2016

MATCH PERFECTION FOUNDATION SPF 20 - SHADE 202 NUDE
octinoxate and titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76485-1056
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.278 g in 30 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.374 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
TALC (UNII: 7SEV7J4R1U)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
QUATERNIUM-91 (UNII: 00J8H295NB)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
MICA (UNII: V8A1AW0880)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
MONTMORILLONITE (UNII: A585MN1H2L)
AMMONIA (UNII: 5138Q19F1X)
CHLORPHENESIN (UNII: I670DAL4SZ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
ALCOHOL (UNII: 3K9958V90M)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DECETH-6 (UNII: P4OYN7A2O9)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
LAURETH-4 (UNII: 6HQ855798J)
LAURETH-30 (UNII: W9D845551A)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:76485-1056-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	01/01/2016	10/01/2020

MATCH PERFECTION FOUNDATION SPF 20 - SHADE 203 TRUE BEIGE
octinoxate and titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76485-1057
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.278 g in 30 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.374 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
TALC (UNII: 7SEV7J4R1U)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
QUATERNIUM-91 (UNII: 00J8H295NB)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
MICA (UNII: V8A1AW0880)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
MONTMORILLONITE (UNII: A585MN1H2L)
AMMONIA (UNII: 5138Q19F1X)
CHLORPHENESIN (UNII: I670DAL4SZ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
ALCOHOL (UNII: 3K9958V90M)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DECETH-6 (UNII: P4OYN7A2O9)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
LAURETH-4 (UNII: 6HQ855798J)
LAURETH-30 (UNII: W9D845551A)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:76485-1057-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	01/01/2016	10/01/2020

Labeler - Rimmel Inc. (401011325)

Name	Address	ID/FEI	Business Operations
Establishment
Coty Lancaster S.A.M.		401011325	manufacture(76485-1050, 76485-1058, 76485-1059, 76485-1060, 76485-1061, 76485-1062, 76485-1051, 76485-1052, 76485-1053, 76485-1054, 76485-1063, 76485-1055, 76485-1056, 76485-1057) , label(76485-1050, 76485-1058, 76485-1059, 76485-1060, 76485-1061, 76485-1062, 76485-1051, 76485-1052, 76485-1053, 76485-1054, 76485-1063, 76485-1055, 76485-1056, 76485-1057)

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Published Date (What is this?)	Version	Files
Oct 27, 2020	5 (current)	download
Feb 11, 2020	4	download
Feb 25, 2019	3	download
Dec 28, 2018	2	download
Jan 4, 2016	1	download

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	NDC
1	76485-1050-1
2	76485-1051-1 (inactivated)
3	76485-1052-1
4	76485-1053-1
5	76485-1054-1
6	76485-1054-2
7	76485-1055-1 (inactivated)
8	76485-1056-1
9	76485-1057-1
10	76485-1058-1
11	76485-1059-1
12	76485-1060-1
13	76485-1061-1
14	76485-1062-1
15	76485-1063-1

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Number of versions: 5

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If this SPL contains inactivated NDCs listed by the FDA initiated compliance action, they will be specified as such.