RIMMEL LASTING BREATHABLE FOUNDATION SPF 20- octinoxate liquid

Rimmel Lasting Breathable Foundation SPF 20 by

Drug Labeling and Warnings

Rimmel Lasting Breathable Foundation SPF 20 by is a Otc medication manufactured, distributed, or labeled by Rimmel Inc., Coty Lancaster S.A.M.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Octinoxate 4%

Purpose

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 SPF value of 15 or higher and other sun protection measures including: [bullet] limit time in the sun, especially from 10 a.m.-2 p.m. [bullet] 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

WATER, CYCLOPENTASILOXANE, TALC, ISODODECANE, GLYCERIN, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, PHENYL TRIMETHICONE, PEG-10 DIMETHICONE, TRIMETHYLSILOXYSILICATE, SODIUM CHLORIDE, AMMONIUM ACRYLATES COPOLYMER, PHENOXYETHANOL, DISTEARDIMONIUM HECTORITE, PENTYLENE GLYCOL, TRIETHOXYCAPRYLYLSILANE, CHLORPHENESIN, FRAGRANCE, ALCOHOL DENAT., ASCORBYL PALMITATE, CITRIC ACID, FRUCTOSE, PROPYLENE CARBONATE, SODIUM HYDROXIDE, TOCOPHERYL ACETATE, UREA, RETINYL PALMITATE, DISODIUM DECETH-6 SULFOSUCCINATE, DISODIUM EDTA, LAURETH-30, ALLANTOIN, MALTOSE, SODIUM LACTATE, SODIUM PCA, TREHALOSE, SODIUM DEHYDROACETATE, BHT, GLUCOSE, SODIUM HYALURONATE, TOCOPHEROL, [May Contain: TITANIUM DIOXIDE, IRON OXIDES]

Questions or comments?

Call 1-800-715-4023

9:00 am to 5:00 pm ET

Monday - Friday

PRINCIPAL DISPLAY PANEL

RIMMEL

LONDON

LASTING

FINISH 25 HR

BREATHABLE

LONG WEAR FOUNDATION

HIGH DEFINITION FINISH

MEDIUM COVERAGE

BROAD SPECTRUM

SPF 20 SUNSCREEN

1 fl oz 30 ml

INGREDIENTS AND APPEARANCE

RIMMEL LASTING BREATHABLE FOUNDATION SPF 20 
octinoxate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76485-1111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ISODODECANE (UNII: A8289P68Y2)
GLYCERIN (UNII: PDC6A3C0OX)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
TALC (UNII: 7SEV7J4R1U)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CHLORPHENESIN (UNII: I670DAL4SZ)
ASCORBYL PALMITATE (UNII: QN83US2B0N)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM LACTATE (UNII: TU7HW0W0QT)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
WATER (UNII: 059QF0KO0R)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
ALLANTOIN (UNII: 344S277G0Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76485-1111-0	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2019
2	NDC: 76485-1111-9	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2019
3	NDC: 76485-1111-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2019
4	NDC: 76485-1111-2	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2019
5	NDC: 76485-1111-4	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2019
6	NDC: 76485-1111-5	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2019
7	NDC: 76485-1111-6	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2019
8	NDC: 76485-1111-7	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2019
9	NDC: 76485-1111-8	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2019
10	NDC: 76485-1111-3	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	03/15/2019

Labeler - Rimmel Inc. (401011325)

Establishment
Name	Address	ID/FEI	Business Operations
Coty Lancaster S.A.M.		401011325	manufacture(76485-1111)