MATCH PERFECTION SPF 18 LIGHT NUDE 102- octinoxate titanium dioxide liquid

Match Perfection SPF 18 by

Drug Labeling and Warnings

Match Perfection SPF 18 by is a Otc medication manufactured, distributed, or labeled by Rimmel Inc., Lancaster S.A.M.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Octinoxate 4%

Titanium Dioxide 4%

PURPOSE

Sunscreen

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

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.

DOSAGE & ADMINISTRATION

Directions. For sunscreen use: apply liberally 15 minutes before sun exposure. Use a water resistant sunscreen if swimming or sweating. Reapply at least every 2 hours.

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 SAFETY INFORMATION

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

INACTIVE INGREDIENT

water, cyclopentasiloxane, butylene glycol, cetyl PEG/PPG-10/1 dimethicone, talc, glycerin, isononyl isononanoate, magnesium sulfate, bis-PEG/PPG-14/14 dimethicone, lecithin, disteardimonium hectorite, laureth-7, silica dimethyl silylate, fragrance, phenoxyethanol, chlorphenesin, dimethiconol, dimethicone crosspolymer, disodium stearoyl glutamate, propylene carbonate, xanthan gum, tocopheryl acetate, disodium edta, aluminum hydroxide, hexyl cinnamal, limonene, sapphare powder, butylphenyl methylpropional, benzyl salicylate, linalool, geraniol, BHT, alpha-isomethyl ionone, citronellol, may contain: titanium dioxide, iron oxides, ultramarines.

Light Nude 102

Back Label/Drug Facts Box

INGREDIENTS AND APPEARANCE

MATCH PERFECTION SPF 18  LIGHT NUDE 102
octinoxate titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76485-1028
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.2 mL  in 30 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1.5 mL  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 1.5) (UNII: V2W71V8T0X)
TALC (UNII: 7SEV7J4R1U)
GLYCERIN (UNII: PDC6A3C0OX)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
MAGNESIUM SULFATE (UNII: DE08037SAB)
LAURETH-7 (UNII: Z95S6G8201)
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CHLORPHENESIN (UNII: I670DAL4SZ)
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
XANTHAN GUM (UNII: TTV12P4NEE)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
GERANIOL (UNII: L837108USY)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FERRIC OXIDE RED (UNII: 1K09F3G675)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76485-1028-1	30 mL in 1 BOTTLE, DISPENSING

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	09/15/2012

Labeler - Rimmel Inc. (949791073)

Establishment
Name	Address	ID/FEI	Business Operations
Lancaster S.A.M.		401011325	manufacture(76485-1028)