LBEL FILLING EFFECT FOUNDATION SPF 10 description, usages, side effects, indications, overdosage, supplying and lots more!

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LBEL FILLING EFFECT FOUNDATION SPF 10

Ventura International LTD

L'BEL FILLING EFFECT FOUNDATION SPF 10


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active Ingredients

Octinoxate 7 %

Purpose

Sunscreen

LBEL FILLING EFFECT FOUNDATION SPF 10 Uses

  • Helps prevent sunburn

Warnings

  • Skin Cancer / Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging.This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.
  • 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

  • Apply liberally and evenly 15 minutes before sun exposure.
  • Reapply at least every 2 hours
  • Use a water resistant sunscreen if swimming or sweating.
  • Children under 6 months of age: Ask a doctor

LBEL FILLING EFFECT FOUNDATION SPF 10 Other information

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

Inactive ingredients

AQUA (WATER), CYCLOMETHICONE, CYCLOPENTASILOXANE, CYCLOHEXASILOXANE, SODIUM CHLORIDE, PEG/PPG-18/18 DIMETHICONE, DIMETHICONE, NYLON-12 FLUORESCENT BRIGHTENER 230 SALT, DIMETHICONOL, DIAZOLIDINYL UREA, CETEARYL DIMETHICONE CROSSPOLYMER, METHYLPARABEN, PARFUM (FRAGRANCE), PROPYLPARABEN, POLYVINYLALCOHOL CROSSPOLYMER, SODIUM HYALURONATE.

MAY CONTAIN

TITANIUM DIOXIDE (CI 77891), IRON OXIDES (CI 77492), IRON OXIDES (CI 77499), IRON OXIDES (CI 77491), METHICONE

Distributed by Ventura International Ltd. DBA Belcorp USA, San Francisco, CA 94111

PRINCIPAL DISPLAY PANEL - 30 ml Bottle Box - (Claire 1) - Beige

L'BEL

EFFET
PARFAIT

filling effect
foundation SPF 10

30 ml e (1 fl.oz.)

LBEL FILLING EFFECT FOUNDATION SPF 10

PRINCIPAL DISPLAY PANEL - 30 ml Bottle Box - (Claire 2) - Beige

L'BEL

EFFET
PARFAIT

filling effect
foundation SPF 10

30 ml e (1 fl.oz.)

LBEL FILLING EFFECT FOUNDATION SPF 10

PRINCIPAL DISPLAY PANEL - 30 ml Bottle Box - (Claire 3) - Beige

L'BEL

EFFET
PARFAIT

filling effect
foundation SPF 10

30 ml e (1 fl.oz.)

LBEL FILLING EFFECT FOUNDATION SPF 10

PRINCIPAL DISPLAY PANEL - 30 ml Bottle Box - (Claire 4) - Beige

L'BEL

EFFET
PARFAIT

filling effect
foundation SPF 10

30 ml e (1 fl.oz.)

LBEL FILLING EFFECT FOUNDATION SPF 10

PRINCIPAL DISPLAY PANEL - 30 ml Bottle Box - (Medium 5) - Brown

L'BEL

EFFET
PARFAIT

filling effect
foundation SPF 10

30 ml e (1 fl.oz.)

LBEL FILLING EFFECT FOUNDATION SPF 10

PRINCIPAL DISPLAY PANEL - 30 ml Bottle Box - (Medium 6) - Brown

L'BEL

EFFET
PARFAIT

filling effect
foundation SPF 10

30 ml e (1 fl.oz.)

LBEL FILLING EFFECT FOUNDATION SPF 10

PRINCIPAL DISPLAY PANEL - 30 ml Bottle Box - (Medium 7) - Brown

L'BEL

EFFET
PARFAIT

filling effect
foundation SPF 10

30 ml e (1 fl.oz.)

LBEL FILLING EFFECT FOUNDATION SPF 10

PRINCIPAL DISPLAY PANEL - 30 ml Bottle Box - (Obscure 8) - Brown

L'BEL

EFFET
PARFAIT

filling effect
foundation SPF 10

30 ml e (1 fl.oz.)

LBEL FILLING EFFECT FOUNDATION SPF 10

PRINCIPAL DISPLAY PANEL - 30 ml Bottle Box - (Obscure 9) - Brown

L'BEL

EFFET
PARFAIT

filling effect
foundation SPF 10

30 ml e (1 fl.oz.)

LBEL FILLING EFFECT FOUNDATION SPF 10

LBEL FILLING EFFECT FOUNDATION SPF 10

Octinoxate LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:14783-200
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 0.07 g

Inactive Ingredients

Ingredient Name Strength
water
cyclomethicone
CYCLOMETHICONE 5
CYCLOMETHICONE 6
SODIUM CHLORIDE
PEG/PPG-18/18 DIMETHICONE
DIMETHICONE
DIAZOLIDINYL UREA
METHYLPARABEN
PROPYLPARABEN
HYALURONATE SODIUM
titanium dioxide
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
ferric oxide red

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:14783-200-01 30 in 1 BOTTLE
2 NDC:14783-200-03 3 in 1 TUBE
3 NDC:14783-200-04 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2013-12-16


LBEL FILLING EFFECT FOUNDATION SPF 10

Octinoxate LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:14783-201
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 0.07 g

Inactive Ingredients

Ingredient Name Strength
water
cyclomethicone
CYCLOMETHICONE 5
CYCLOMETHICONE 6
SODIUM CHLORIDE
PEG/PPG-18/18 DIMETHICONE
DIMETHICONE
DIAZOLIDINYL UREA
METHYLPARABEN
PROPYLPARABEN
HYALURONATE SODIUM
titanium dioxide
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
ferric oxide red

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:14783-201-05 30 in 1 BOTTLE
2 NDC:14783-201-07 3 in 1 TUBE
3 NDC:14783-201-08 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2013-12-16


LBEL FILLING EFFECT FOUNDATION SPF 10

Octinoxate LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:14783-202
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 0.07 g

Inactive Ingredients

Ingredient Name Strength
water
cyclomethicone
CYCLOMETHICONE 5
CYCLOMETHICONE 6
SODIUM CHLORIDE
PEG/PPG-18/18 DIMETHICONE
DIMETHICONE
DIAZOLIDINYL UREA
METHYLPARABEN
PROPYLPARABEN
HYALURONATE SODIUM
titanium dioxide
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
ferric oxide red

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:14783-202-09 30 in 1 BOTTLE
2 NDC:14783-202-11 3 in 1 TUBE
3 NDC:14783-202-12 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2013-12-16


LBEL FILLING EFFECT FOUNDATION SPF 10

Octinoxate LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:14783-203
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 0.07 g

Inactive Ingredients

Ingredient Name Strength
water
cyclomethicone
CYCLOMETHICONE 5
CYCLOMETHICONE 6
SODIUM CHLORIDE
PEG/PPG-18/18 DIMETHICONE
DIMETHICONE
DIAZOLIDINYL UREA
METHYLPARABEN
PROPYLPARABEN
HYALURONATE SODIUM
titanium dioxide
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
ferric oxide red

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:14783-203-13 30 in 1 BOTTLE
2 NDC:14783-203-15 3 in 1 TUBE
3 NDC:14783-203-16 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2013-12-16


LBEL FILLING EFFECT FOUNDATION SPF 10

Octinoxate LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:14783-204
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 0.07 g

Inactive Ingredients

Ingredient Name Strength
water
cyclomethicone
CYCLOMETHICONE 5
CYCLOMETHICONE 6
SODIUM CHLORIDE
PEG/PPG-18/18 DIMETHICONE
DIMETHICONE
DIAZOLIDINYL UREA
METHYLPARABEN
PROPYLPARABEN
HYALURONATE SODIUM
titanium dioxide
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
ferric oxide red

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:14783-204-17 30 in 1 BOTTLE
2 NDC:14783-204-19 3 in 1 TUBE
3 NDC:14783-204-20 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2013-12-16


LBEL FILLING EFFECT FOUNDATION SPF 10

Octinoxate LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:14783-205
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 0.07 g

Inactive Ingredients

Ingredient Name Strength
water
cyclomethicone
CYCLOMETHICONE 5
CYCLOMETHICONE 6
SODIUM CHLORIDE
PEG/PPG-18/18 DIMETHICONE
DIMETHICONE
DIAZOLIDINYL UREA
METHYLPARABEN
PROPYLPARABEN
HYALURONATE SODIUM
titanium dioxide
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
ferric oxide red

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:14783-205-21 30 in 1 BOTTLE
2 NDC:14783-205-23 3 in 1 TUBE
3 NDC:14783-205-24 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2013-12-16


LBEL FILLING EFFECT FOUNDATION SPF 10

Octinoxate LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:14783-206
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 0.07 g

Inactive Ingredients

Ingredient Name Strength
water
cyclomethicone
CYCLOMETHICONE 5
CYCLOMETHICONE 6
SODIUM CHLORIDE
PEG/PPG-18/18 DIMETHICONE
DIMETHICONE
DIAZOLIDINYL UREA
METHYLPARABEN
PROPYLPARABEN
HYALURONATE SODIUM
titanium dioxide
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
ferric oxide red

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:14783-206-25 30 in 1 BOTTLE
2 NDC:14783-206-27 3 in 1 TUBE
3 NDC:14783-206-28 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2013-12-16


LBEL FILLING EFFECT FOUNDATION SPF 10

Octinoxate LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:14783-207
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 0.07 g

Inactive Ingredients

Ingredient Name Strength
water
cyclomethicone
CYCLOMETHICONE 5
CYCLOMETHICONE 6
SODIUM CHLORIDE
PEG/PPG-18/18 DIMETHICONE
DIMETHICONE
DIAZOLIDINYL UREA
METHYLPARABEN
PROPYLPARABEN
HYALURONATE SODIUM
titanium dioxide
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
ferric oxide red

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:14783-207-29 30 in 1 BOTTLE
2 NDC:14783-207-31 3 in 1 TUBE
3 NDC:14783-207-32 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2013-12-16


LBEL FILLING EFFECT FOUNDATION SPF 10

Octinoxate LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:14783-208
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 0.07 g

Inactive Ingredients

Ingredient Name Strength
water
cyclomethicone
CYCLOMETHICONE 5
CYCLOMETHICONE 6
SODIUM CHLORIDE
PEG/PPG-18/18 DIMETHICONE
DIMETHICONE
DIAZOLIDINYL UREA
METHYLPARABEN
PROPYLPARABEN
HYALURONATE SODIUM
titanium dioxide
FERRIC OXIDE YELLOW
FERROSOFERRIC OXIDE
ferric oxide red

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:14783-208-33 30 in 1 BOTTLE
2 NDC:14783-208-35 3 in 1 TUBE
3 NDC:14783-208-36 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2013-12-16


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Be sure to consult your doctor before taking any medication!
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