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LBEL EFFET PARFAIT filling effect foundation SPF 10 - MEDIUM 7 (Ventura Corporation LTD.)

Available Formats

Dosage Form Package Information Links
LIQUID 1 BOTTLE in 1 BOX (13537-566-02) > 30 mL in 1 BOTTLE (13537-566-01) Label Information

Complete LBEL EFFET PARFAIT filling effect foundation SPF 10 - MEDIUM 7 Information

  • Active Ingredients

    Octinoxate 7.0 %


  • Purpose

    sunscreen


  • Uses

    • Helps prevent sunburn.
    • Higher SPF gives more sunburn protection.
    • Provides minimal protection against sunburn.

  • Warnings

    • For external use only.

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

    • Stop use and ask a doctor if rash or irritation develops and lasts.

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

  • Directions

    • Apply liberally before sun exposure and as needed.

  • Other information

    • Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreen may reduce the risk of skin aging, skin cancer, and other harmful effects of the sun.
    • Apply to the forehead, nose, chin and both cheeks. Blend with circular motion and spread softly without stretching the skin.

  • Inactive ingredients

    Aqua (water), cyclomethicone, cyclopentasiloxane, cyclohexasiloxane, sodium chloride, peg/ppg-18/18 dimethicone, dimethicone, nylon-12 fluorescent brightener 230 salt, dimethiconol, diazolidinyl urea, methicone, cetearyl dimethicone crosspolymer, methylparaben, parfum (fragrance), propylparaben, polyvinylalcohol crosspolymer, sodium hyaluronate
    May contain: CI 77891 (titanium dioxide), CI 77492 (iron oxides), CI 77491 (iron oxides), CI 77499 (iron oxides).


  • SPL UNCLASSIFIED SECTION

    PR: Distributed by Ventura Corporation, Ltd. San Juan, Puerto Rico 00926.


  • PRINCIPAL DISPLAY PANEL - 30 ml Bottle Box - CLAIRE 1

    L'BEL

    EFFET
    PARFAIT

    filling effect
    foundation SPF 10

    30 ml e (1 fl.oz.)

    Principal Display Panel - 30 ml Bottle Box - CLAIRE 1

  • PRINCIPAL DISPLAY PANEL - 30 ml Bottle Box - CLAIRE 2

    L'BEL

    EFFET
    PARFAIT

    filling effect
    foundation SPF 10

    30 ml e (1 fl.oz.)

    Principal Display Panel - 30 ml Bottle Box - CLAIRE 2

  • PRINCIPAL DISPLAY PANEL - 30 ml Bottle Box - CLAIRE 3

    L'BEL

    EFFET
    PARFAIT

    filling effect
    foundation SPF 10

    30 ml e (1 fl.oz.)

    Principal Display Panel - 30 ml Bottle Box - CLAIRE 3

  • PRINCIPAL DISPLAY PANEL - 30 ml Bottle Box - CLAIRE 4

    L'BEL

    EFFET
    PARFAIT

    filling effect
    foundation SPF 10

    30 ml e (1 fl.oz.)

    Principal Display Panel - 30 ml Bottle Box - CLAIRE 4

  • PRINCIPAL DISPLAY PANEL - 30 ml Bottle Box - MEDIUM 5

    L'BEL

    EFFET
    PARFAIT

    filling effect
    foundation SPF 10

    30 ml e (1 fl.oz.)

    Principal Display Panel - 30 ml Bottle Box - MEDIUM 5

  • PRINCIPAL DISPLAY PANEL - 30 ml Bottle Box - MEDIUM 6

    L'BEL

    EFFET
    PARFAIT

    filling effect
    foundation SPF 10

    30 ml e (1 fl.oz.)

    Principal Display Panel - 30 ml Bottle Box - MEDIUM 6

  • PRINCIPAL DISPLAY PANEL - 30 ml Bottle Box - MEDIUM 7

    L'BEL

    EFFET
    PARFAIT

    filling effect
    foundation SPF 10

    30 ml e (1 fl.oz.)

    Principal Display Panel - 30 ml Bottle Box - MEDIUM 7

  • PRINCIPAL DISPLAY PANEL - 30 ml Bottle Box - OBSCURE 8

    L'BEL

    EFFET
    PARFAIT

    filling effect
    foundation SPF 10

    30 ml e (1 fl.oz.)

    Principal Display Panel - 30 ml Bottle Box - OBSCURE 8

  • PRINCIPAL DISPLAY PANEL - 30 ml Bottle Box - OBSCURE 9

    L'BEL

    EFFET
    PARFAIT

    filling effect
    foundation SPF 10

    30 ml e (1 fl.oz.)

    Principal Display Panel - 30 ml Bottle Box - OBSCURE 9

  • INGREDIENTS AND APPEARANCE
    LBEL EFFET PARFAIT FILLING EFFECT FOUNDATION SPF 10 - CLAIRE 1 
    octinoxate liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:13537-560
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 0.07 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    water (UNII: 059QF0KO0R)  
    cyclomethicone (UNII: NMQ347994Z)  
    cyclomethicone 5 (UNII: 0THT5PCI0R)  
    cyclomethicone 6 (UNII: XHK3U310BA)  
    sodium chloride (UNII: 451W47IQ8X)  
    peg/ppg-18/18 dimethicone (UNII: 9H0AO7T794)  
    dimethicone (UNII: 92RU3N3Y1O)  
    diazolidinyl urea (UNII: H5RIZ3MPW4)  
    methylparaben (UNII: A2I8C7HI9T)  
    propylparaben (UNII: Z8IX2SC1OH)  
    hyaluronate sodium (UNII: YSE9PPT4TH)  
    titanium dioxide (UNII: 15FIX9V2JP)  
    ferric oxide yellow (UNII: EX438O2MRT)  
    ferric oxide red (UNII: 1K09F3G675)  
    ferrosoferric oxide (UNII: XM0M87F357)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:13537-560-02 1 in 1 BOX
    1 NDC:13537-560-01 30 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part352 05/07/2013
    LBEL EFFET PARFAIT FILLING EFFECT FOUNDATION SPF 10 - CLAIRE 2 
    octinoxate liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:13537-561
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 0.07 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    water (UNII: 059QF0KO0R)  
    cyclomethicone (UNII: NMQ347994Z)  
    cyclomethicone 5 (UNII: 0THT5PCI0R)  
    cyclomethicone 6 (UNII: XHK3U310BA)  
    sodium chloride (UNII: 451W47IQ8X)  
    peg/ppg-18/18 dimethicone (UNII: 9H0AO7T794)  
    dimethicone (UNII: 92RU3N3Y1O)  
    diazolidinyl urea (UNII: H5RIZ3MPW4)  
    methylparaben (UNII: A2I8C7HI9T)  
    propylparaben (UNII: Z8IX2SC1OH)  
    hyaluronate sodium (UNII: YSE9PPT4TH)  
    titanium dioxide (UNII: 15FIX9V2JP)  
    ferric oxide yellow (UNII: EX438O2MRT)  
    ferric oxide red (UNII: 1K09F3G675)  
    ferrosoferric oxide (UNII: XM0M87F357)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:13537-561-02 1 in 1 BOX
    1 NDC:13537-561-01 30 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part352 05/07/2013
    LBEL EFFET PARFAIT FILLING EFFECT FOUNDATION SPF 10 - CLAIRE 3 
    octinoxate liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:13537-562
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 0.07 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    water (UNII: 059QF0KO0R)  
    cyclomethicone (UNII: NMQ347994Z)  
    cyclomethicone 5 (UNII: 0THT5PCI0R)  
    cyclomethicone 6 (UNII: XHK3U310BA)  
    sodium chloride (UNII: 451W47IQ8X)  
    peg/ppg-18/18 dimethicone (UNII: 9H0AO7T794)  
    dimethicone (UNII: 92RU3N3Y1O)  
    diazolidinyl urea (UNII: H5RIZ3MPW4)  
    methylparaben (UNII: A2I8C7HI9T)  
    propylparaben (UNII: Z8IX2SC1OH)  
    hyaluronate sodium (UNII: YSE9PPT4TH)  
    titanium dioxide (UNII: 15FIX9V2JP)  
    ferric oxide yellow (UNII: EX438O2MRT)  
    ferric oxide red (UNII: 1K09F3G675)  
    ferrosoferric oxide (UNII: XM0M87F357)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:13537-562-02 1 in 1 BOX
    1 NDC:13537-562-01 30 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part352 05/07/2013
    LBEL EFFET PARFAIT FILLING EFFECT FOUNDATION SPF 10 - CLAIRE 4 
    octinoxate liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:13537-563
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 0.07 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    water (UNII: 059QF0KO0R)  
    cyclomethicone (UNII: NMQ347994Z)  
    cyclomethicone 5 (UNII: 0THT5PCI0R)  
    cyclomethicone 6 (UNII: XHK3U310BA)  
    sodium chloride (UNII: 451W47IQ8X)  
    peg/ppg-18/18 dimethicone (UNII: 9H0AO7T794)  
    dimethicone (UNII: 92RU3N3Y1O)  
    diazolidinyl urea (UNII: H5RIZ3MPW4)  
    methylparaben (UNII: A2I8C7HI9T)  
    propylparaben (UNII: Z8IX2SC1OH)  
    hyaluronate sodium (UNII: YSE9PPT4TH)  
    titanium dioxide (UNII: 15FIX9V2JP)  
    ferric oxide yellow (UNII: EX438O2MRT)  
    ferric oxide red (UNII: 1K09F3G675)  
    ferrosoferric oxide (UNII: XM0M87F357)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:13537-563-02 1 in 1 BOX
    1 NDC:13537-563-01 30 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part352 05/07/2013
    LBEL EFFET PARFAIT FILLING EFFECT FOUNDATION SPF 10 - MEDIUM 5 
    octinoxate liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:13537-564
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 0.07 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    water (UNII: 059QF0KO0R)  
    cyclomethicone (UNII: NMQ347994Z)  
    cyclomethicone 5 (UNII: 0THT5PCI0R)  
    cyclomethicone 6 (UNII: XHK3U310BA)  
    sodium chloride (UNII: 451W47IQ8X)  
    peg/ppg-18/18 dimethicone (UNII: 9H0AO7T794)  
    dimethicone (UNII: 92RU3N3Y1O)  
    diazolidinyl urea (UNII: H5RIZ3MPW4)  
    methylparaben (UNII: A2I8C7HI9T)  
    propylparaben (UNII: Z8IX2SC1OH)  
    hyaluronate sodium (UNII: YSE9PPT4TH)  
    titanium dioxide (UNII: 15FIX9V2JP)  
    ferric oxide yellow (UNII: EX438O2MRT)  
    ferric oxide red (UNII: 1K09F3G675)  
    ferrosoferric oxide (UNII: XM0M87F357)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:13537-564-02 1 in 1 BOX
    1 NDC:13537-564-01 30 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part352 05/07/2013
    LBEL EFFET PARFAIT FILLING EFFECT FOUNDATION SPF 10 - MEDIUM 6 
    octinoxate liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:13537-565
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 0.07 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    water (UNII: 059QF0KO0R)  
    cyclomethicone (UNII: NMQ347994Z)  
    cyclomethicone 5 (UNII: 0THT5PCI0R)  
    cyclomethicone 6 (UNII: XHK3U310BA)  
    sodium chloride (UNII: 451W47IQ8X)  
    peg/ppg-18/18 dimethicone (UNII: 9H0AO7T794)  
    dimethicone (UNII: 92RU3N3Y1O)  
    diazolidinyl urea (UNII: H5RIZ3MPW4)  
    methylparaben (UNII: A2I8C7HI9T)  
    propylparaben (UNII: Z8IX2SC1OH)  
    hyaluronate sodium (UNII: YSE9PPT4TH)  
    titanium dioxide (UNII: 15FIX9V2JP)  
    ferric oxide yellow (UNII: EX438O2MRT)  
    ferric oxide red (UNII: 1K09F3G675)  
    ferrosoferric oxide (UNII: XM0M87F357)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:13537-565-02 1 in 1 BOX
    1 NDC:13537-565-01 30 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part352 05/07/2013
    LBEL EFFET PARFAIT FILLING EFFECT FOUNDATION SPF 10 - MEDIUM 7 
    octinoxate liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:13537-566
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 0.07 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    water (UNII: 059QF0KO0R)  
    cyclomethicone (UNII: NMQ347994Z)  
    cyclomethicone 5 (UNII: 0THT5PCI0R)  
    cyclomethicone 6 (UNII: XHK3U310BA)  
    sodium chloride (UNII: 451W47IQ8X)  
    peg/ppg-18/18 dimethicone (UNII: 9H0AO7T794)  
    dimethicone (UNII: 92RU3N3Y1O)  
    diazolidinyl urea (UNII: H5RIZ3MPW4)  
    methylparaben (UNII: A2I8C7HI9T)  
    propylparaben (UNII: Z8IX2SC1OH)  
    hyaluronate sodium (UNII: YSE9PPT4TH)  
    titanium dioxide (UNII: 15FIX9V2JP)  
    ferric oxide yellow (UNII: EX438O2MRT)  
    ferric oxide red (UNII: 1K09F3G675)  
    ferrosoferric oxide (UNII: XM0M87F357)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:13537-566-02 1 in 1 BOX
    1 NDC:13537-566-01 30 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part352 05/07/2013
    LBEL EFFET PARFAIT FILLING EFFECT FOUNDATION SPF 10 - OBSCURE 8 
    octinoxate liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:13537-567
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 0.07 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    water (UNII: 059QF0KO0R)  
    cyclomethicone (UNII: NMQ347994Z)  
    cyclomethicone 5 (UNII: 0THT5PCI0R)  
    cyclomethicone 6 (UNII: XHK3U310BA)  
    sodium chloride (UNII: 451W47IQ8X)  
    peg/ppg-18/18 dimethicone (UNII: 9H0AO7T794)  
    dimethicone (UNII: 92RU3N3Y1O)  
    diazolidinyl urea (UNII: H5RIZ3MPW4)  
    methylparaben (UNII: A2I8C7HI9T)  
    propylparaben (UNII: Z8IX2SC1OH)  
    hyaluronate sodium (UNII: YSE9PPT4TH)  
    titanium dioxide (UNII: 15FIX9V2JP)  
    ferric oxide yellow (UNII: EX438O2MRT)  
    ferric oxide red (UNII: 1K09F3G675)  
    ferrosoferric oxide (UNII: XM0M87F357)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:13537-567-02 1 in 1 BOX
    1 NDC:13537-567-01 30 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part352 05/07/2013
    LBEL EFFET PARFAIT FILLING EFFECT FOUNDATION SPF 10 - OBSCURE 9 
    octinoxate liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:13537-568
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 0.07 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    water (UNII: 059QF0KO0R)  
    cyclomethicone (UNII: NMQ347994Z)  
    cyclomethicone 5 (UNII: 0THT5PCI0R)  
    cyclomethicone 6 (UNII: XHK3U310BA)  
    sodium chloride (UNII: 451W47IQ8X)  
    peg/ppg-18/18 dimethicone (UNII: 9H0AO7T794)  
    dimethicone (UNII: 92RU3N3Y1O)  
    diazolidinyl urea (UNII: H5RIZ3MPW4)  
    methylparaben (UNII: A2I8C7HI9T)  
    propylparaben (UNII: Z8IX2SC1OH)  
    hyaluronate sodium (UNII: YSE9PPT4TH)  
    titanium dioxide (UNII: 15FIX9V2JP)  
    ferric oxide yellow (UNII: EX438O2MRT)  
    ferric oxide red (UNII: 1K09F3G675)  
    ferrosoferric oxide (UNII: XM0M87F357)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:13537-568-02 1 in 1 BOX
    1 NDC:13537-568-01 30 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part352 05/07/2013
    Labeler - Ventura Corporation LTD. (602751344)
    Establishment
    Name Address ID/FEI Business Operations
    Bel Star S.A. (Colombia) 880160197 MANUFACTURE(13537-560, 13537-561, 13537-562, 13537-563, 13537-564, 13537-565, 13537-566, 13537-567, 13537-568)