Ventura Corporation LTD
L'BEL REPLENISHING FOUNDATION SPF 14
FULL PRESCRIBING INFORMATION: CONTENTS*
FULL PRESCRIBING INFORMATION
Drug Facts
Active Ingredients
Octinoxate (4.5 %)
Purpose
Sunscreen
LBEL REPLENISHING FOUNDATION SPF 14 Uses
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.
-
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
- Apply to the forehead, nose, chin and both cheeks.
Blend with CIrcular motion and spread softly without stretching the skin.
LBEL REPLENISHING FOUNDATION SPF 14 Other information
- Protect the product in this container from excessive heat and direct sun.
Inactive ingredients
Water, cyclopentasiloxane, butylene glycol, cyclohexasiloxane, phenyl trimethicone, cetyl peg/ppg-10/1 dimethicone, polyglyceryl-4 isostearate, nylon-12 fluorescent brightener 230 salt, hexyl laurate, mannitol, glycerin, ethylene/acrylic acid copolymer, glycine soja (soybean) protein, peg/ppg-18/18 dimethicone, disteardimonium hectorite, sodium chloride, dimethicone, propylene glycol, dimethicone crosspolymer, dimethicone/vinyl dimethicone crosspolymer, diazolidinyl urea, hydrolyzed keratin, dimethiconol, sucrose, methylparaben, serine, fragrance, arginine, cyclodextrin, polyvinylalcohol crosspolymer, pca, bht, macrocystis pyrifera extract, yeast extract, alanine, propylparaben, hydrolyzed wheat protein, carbomer, pvp, threonine, polysorbate 20, disodium succinate, mourera fluviatilis extract, palmitoyl pentapeptide-4.
May contain: titanium dioxide, iron oxides, iron oxides, iron oxides,methicone.
PR: Distributed by Ventura Corporation, Ltd. San Juan, Puerto Rico 00926.
PRINCIPAL DISPLAY PANEL - 30 g Bottle Box - Claire 1 - BEIGE
L'BEL
replenishing foundation SPF 14
Net Weight 1 oz. (30 g)
PRINCIPAL DISPLAY PANEL - 30 g Bottle Box - Claire 2 - BEIGE
L'BEL
replenishing foundation SPF 14
Net Weight 1 oz. (30 g)
PRINCIPAL DISPLAY PANEL - 30 g Bottle Box - Claire 3 - BEIGE
L'BEL
replenishing foundation SPF 14
Net Weight 1 oz. (30 g)
PRINCIPAL DISPLAY PANEL - 30 g Bottle Box - Claire 4 - BEIGE
L'BEL
replenishing foundation SPF 14
Net Weight 1 oz. (30 g)
PRINCIPAL DISPLAY PANEL - 30 g Bottle Box - Medium 5 - BROWN
L'BEL
replenishing foundation SPF 14
Net Weight 1 oz. (30 g)
PRINCIPAL DISPLAY PANEL - 30 g Bottle Box - Medium 6 - BROWN
L'BEL
replenishing foundation SPF 14
Net Weight 1 oz. (30 g)
PRINCIPAL DISPLAY PANEL - 30 g Bottle Box - Medium 7 - BROWN
L'BEL
replenishing foundation SPF 14
Net Weight 1 oz. (30 g)
PRINCIPAL DISPLAY PANEL - 30 g Bottle Box - Obscure 8 - BROWN
L'BEL
replenishing foundation SPF 14
Net Weight 1 oz. (30 g)
PRINCIPAL DISPLAY PANEL - 30 g Bottle Box - Obscure 9 - BROWN
L'BEL
replenishing foundation SPF 14
Net Weight 1 oz. (30 g)
LBEL REPLENISHING FOUNDATION SPF 14
Octinoxate LIQUID
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:13537-257 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
0.045 g
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
NDC:13537-257-01 |
30 in 1 BOTTLE |
|
|
|
2 |
NDC:13537-257-02 |
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 REPLENISHING FOUNDATION SPF 14
Octinoxate LIQUID
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:13537-258 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
0.045 g
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
NDC:13537-258-03 |
30 in 1 BOTTLE |
|
|
|
2 |
NDC:13537-258-04 |
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 REPLENISHING FOUNDATION SPF 14
Octinoxate LIQUID
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:13537-259 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
0.045 g
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
NDC:13537-259-05 |
30 in 1 BOTTLE |
|
|
|
2 |
NDC:13537-259-06 |
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 REPLENISHING FOUNDATION SPF 14
Octinoxate LIQUID
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:13537-260 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
0.045 g
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
NDC:13537-260-07 |
30 in 1 BOTTLE |
|
|
|
2 |
NDC:13537-260-08 |
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 REPLENISHING FOUNDATION SPF 14
Octinoxate LIQUID
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:13537-298 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
0.045 g
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
NDC:13537-298-09 |
30 in 1 BOTTLE |
|
|
|
2 |
NDC:13537-298-10 |
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 REPLENISHING FOUNDATION SPF 14
Octinoxate LIQUID
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:13537-262 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
0.045 g
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
NDC:13537-262-11 |
30 in 1 BOTTLE |
|
|
|
2 |
NDC:13537-262-12 |
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 REPLENISHING FOUNDATION SPF 14
Octinoxate LIQUID
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:13537-263 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
0.045 g
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
NDC:13537-263-13 |
30 in 1 BOTTLE |
|
|
|
2 |
NDC:13537-263-14 |
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 REPLENISHING FOUNDATION SPF 14
Octinoxate LIQUID
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:13537-264 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
0.045 g
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
NDC:13537-264-15 |
30 in 1 BOTTLE |
|
|
|
2 |
NDC:13537-264-16 |
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 REPLENISHING FOUNDATION SPF 14
Octinoxate LIQUID
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:13537-265 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
0.045 g
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
NDC:13537-265-17 |
30 in 1 BOTTLE |
|
|
|
2 |
NDC:13537-265-18 |
1 in 1 BOX |
|
|
Marketing Information
|
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
|
part |
part352 |
2013-12-16 |
|
|
