Rimmel Lasting Finish Breathable Foundation SPF 20

Rimmel Lasting Finish Breathable Foundation SPF 20

Drug Labeling and Warnings

Drug Details

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RIMMEL LASTING BREATHABLE FOUNDATION SPF 20- octinoxate liquid 
Rimmel Inc.

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.

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Rimmel Lasting Finish Breathable Foundation SPF 20

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

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

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RIMMEL LASTING BREATHABLE FOUNDATION SPF 20 
octinoxate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 76485-1111
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE4 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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)  
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)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
ALLANTOIN (UNII: 344S277G0Z)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 76485-1111-030 mL in 1 BOTTLE; Type 0: Not a Combination Product03/15/2019
2NDC: 76485-1111-930 mL in 1 BOTTLE; Type 0: Not a Combination Product03/15/2019
3NDC: 76485-1111-130 mL in 1 BOTTLE; Type 0: Not a Combination Product03/15/2019
4NDC: 76485-1111-230 mL in 1 BOTTLE; Type 0: Not a Combination Product03/15/2019
5NDC: 76485-1111-430 mL in 1 BOTTLE; Type 0: Not a Combination Product03/15/2019
6NDC: 76485-1111-530 mL in 1 BOTTLE; Type 0: Not a Combination Product03/15/2019
7NDC: 76485-1111-630 mL in 1 BOTTLE; Type 0: Not a Combination Product03/15/2019
8NDC: 76485-1111-730 mL in 1 BOTTLE; Type 0: Not a Combination Product03/15/2019
9NDC: 76485-1111-830 mL in 1 BOTTLE; Type 0: Not a Combination Product03/15/2019
10NDC: 76485-1111-330 mL in 1 BOTTLE; Type 0: Not a Combination Product03/15/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35203/15/2019
Labeler - Rimmel Inc. (401011325)
Establishment
NameAddressID/FEIBusiness Operations
Coty Lancaster S.A.M.401011325manufacture(76485-1111)

Revised: 3/2019
 
Rimmel Inc.


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