Rimmel London Moisture Renew Lipgloss - Mauve Renew (125)

Dosage form: cream
Ingredients: OCTINOXATE .012mL in 6mL, OCTISALATE .12mL in 6mL
Labeler: Lancaster S.A.M.
NDC Code: 59351-0305

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.

Rimmel London Moisture Renew Lipgloss Mauve Renew (125) SPF 15 Sunscreen

USE: Helps prevent sunburn.

WARNING: Stop use if skin rash occurs.

Active Ingredients: Octinoxate 7.5%, Octisalate 2.0%.






COSMETIC INGREDIENTS: POLYBUTENE, HYDROGENATED
POLYISOBUTENE, PARAFFINUM LIQUIDUM/MINERAL OIL/
HUILE MINERALE, ETHYLHEXYL PALMITATE, LANOLIN OIL,
ETHYLENE/PROPYLENE/STYRENE COPOLYMER, POLYETHYLENE,
CALCIUM ALUMINUM BOROSILICATE, SILICA DIMETHYL
SILYLATE, SILICA, SYNTHETIC FLUORPHLOGOPITE,

ISOPROPYLPARABEN,BUTYLENE/ETHYLENE/STYRENE
COPOLYMER, TOCOPHERYL ACETATE, PENTAERYTHRITYL
TETRAISOSTEARATE, BUTYLPARABEN, ISOBUTYLPARABEN,
PARFUM/FRAGRANCE, TRIBEHENIN, CARMINE, LINALOOL, BHT,
ASCORBYL PALMITATE, RETINYL PALMITATE, TIN OXIDE,
HYDROXYCITRONELLAL, SORBITAN ISOSTEARATE, HEXYL

CINNAMAL, BUTYLENE GLYCOL, PALMITIC ACID,
PHENOXYETHANOL, METHYLPARABEN, SODIUM CHONDROITIN
SULFATE, PROPYLPARABEN, CAPRYLYL GLYCOL, ATELOCOLLAGEN,
SODIUM HYALURONATE, HEXYLENE GLYCOL, PALMITOYL
OLIGOPEPTIDE, ETHYLPARABEN. [MAY CONTAIN/PEUT CONTENIR/
: MICA, TITANIUM DIOXIDE (CI 77891), IRON OXIDES

(CI 77491, CI 77492, CI 77499), DandC RED NO. 7 CALCIUM LAKE
(CI 15850), DandC RED NO. 6 BARIUM LAKE (CI 15850), FDandC
YELLOW NO. 5 ALUMINUM LAKE (CI 19140), DandC RED NO. 33
ALUMINUM LAKE (CI 17200), FDandC BLUE NO. 1 ALUMINUM LAKE
CI 42090), FDandC YELLOW NO. 6 ALUMINUM LAKE (CI 15985),
DandC RED NO. 27 ALUMINUM LAKE (CI 45410)].



RIMMEL LONDON

SPF 15 SUNSCREEN

MOISTURE RENEW

WITH COLLAGEN AND VITAMINS A, C and E

CREAM LIPGLOSS

0.20 fl oz 6 ml





RIMMEL LONDON  MOISTURE RENEW LIPGLOSS - MAUVE RENEW (125)
octinoxate, octisalate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59351-0305
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (OCTINOXATE) OCTINOXATE.012 mL  in 6 mL
OCTISALATE (OCTISALATE) OCTISALATE.12 mL  in 6 mL
Inactive Ingredients
Ingredient NameStrength
MINERAL OIL 
ETHYLHEXYL PALMITATE 
LANOLIN 
ETHYLENE 
ALUMINUM 
SILICON DIOXIDE 
ISOPROPYLPARABEN 
ETHYLENE 
.ALPHA.-TOCOPHEROL ACETATE, D- 
BUTYLPARABEN 
ISOBUTYLPARABEN 
TRIBEHENIN 
LINALOOL, (+/-)-  
BUTYLATED HYDROXYTOLUENE 
ASCORBYL PALMITATE 
VITAMIN A PALMITATE 
STANNIC OXIDE 
HYDROXYCITRONELLAL 
SORBITAN 
.ALPHA.-HEXYLCINNAMALDEHYDE 
BUTYLENE GLYCOL 
PALMITIC ACID 
PHENOXYETHANOL 
METHYLPARABEN 
SULFATE ION 
PROPYLPARABEN 
CAPRYLYL GLYCOL 
HYALURONATE SODIUM 
HEXYLENE GLYCOL 
ETHYLPARABEN 
MICA 
TITANIUM DIOXIDE 
IRON 
CALCIUM 
BARIUM 
Packaging
#Item CodePackage Description
1NDC:59351-0305-16 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35210/20/2010
Labeler - Lancaster S.A.M. (401011325)
Registrant - Rimmel Inc. (965020402)
Establishment
NameAddressID/FEIOperations
Lancaster S.A.M.401011325manufacture

Revised: 10/2010
 
Lancaster S.A.M.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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