Tarte Inc
ReCreate™ foundation with Wrinkle Rewind™ technology
FULL PRESCRIBING INFORMATION: CONTENTS*
FULL PRESCRIBING INFORMATION
Drug Facts
Active ingredient
Purpose
|
Active ingredients
|
Purpose
|
| Octinoxate 7.5% |
Sunscreen |
| Octisalate 4.0% |
Sunscreen |
| Oxybenzone 2.0% |
Sunscreen |
ReCreate Foundation Uses
- helps prevent sunburn.
- higher SPF gives more sun protection.
Warnings
For external use only.
When using this product keep out of eyes. Rinse with water to remove.
Stop use and ask doctor if rash or irritation develops and lasts.
Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Apply evenly over entire face. Apply liberally before sun exposure and as needed.
- Children under 6 months of age: ask a doctor.
ReCreate Foundation Other information
You may report a serious adverse reaction to: tarte, Inc. 53 W 36th Street Suite 902 New York, NY 10018.
Inactive ingredients
water, cyclopentasiloxane, cetyl, PEG/PPG-10/1 dimethicone, butylene glycol, cyclohexasiloxane, ozkerite, silica, VP/elcosene copolymer, disteardimonium hectorite, magnesium sulfate, polyglyceryl-4-isostearate, hexyl laurate, bis-vinyl dimethicone, dimethicone copolymer, phenoxyethanol, acrylates, polytrimethysloxymethacrylate copolymer, beeswax, potassium sorbate, glycereth-18 ethylhexacanoate, boron nitride, polymethylsilsesquioxane, C18-21 alkaine, polyisobutene, ethoxydiglycol, xanthan gum, barium sulfate, C30-45 alkyl cetearyl dimethicone crosspolymer, caprylyl glycol, 1,2-hexanediol, glycereth-18, isododecane, triethoxycaprylylsilane, aluminum dimyrustate, hydrolyzed vegetable protein, propylene carbonate, allantoin, disodium stearoyl glutamate, trehalose, glycerin, hexyfene glycol, gold, peat extract, palmitoyl hexapeptide-14, sodium benzoate, sodium hyaluronate, (+/-); Mica, iron oxides, titanium dioxide.
PRINCIPAL DISPLAY PANEL - 29.5 mL Carton
NEW
FLO-THRU™
pump
tarte™
high-performance naturals™
ReCreate™
foundation with
Wrinkle Rewind™ technology
SPF 15 UVA/UVB Broad Spectrum
Sunscreen
29.5 mL e 1 Fl. Oz.
ReCreate Foundation
Octinoxate, Octisalate, and Oxybenzone CREAM
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:51060-001 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
2.2125 mL
|
|
OCTISALATE OCTISALATE |
|
1.18 mL
|
|
OXYBENZONE OXYBENZONE |
|
.59 mL
|
Product Characteristics
|
|
Color
|
|
BROWN |
|
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
|
29.5 in 1 BOTTLE, PUMP |
|
|
|
2 |
NDC:51060-001-29 |
1 in 1 CARTON |
|
|
Marketing Information
|
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
|
part |
part352 |
2010-06-01 |
|
|
ReCreate Foundation
Octinoxate, Octisalate, and Oxybenzone CREAM
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:51060-002 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
2.2125 mL
|
|
OCTISALATE OCTISALATE |
|
1.18 mL
|
|
OXYBENZONE OXYBENZONE |
|
.59 mL
|
Product Characteristics
|
|
Color
|
|
BROWN |
|
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
|
29.5 in 1 BOTTLE, PUMP |
|
|
|
2 |
NDC:51060-002-92 |
1 in 1 CARTON |
|
|
Marketing Information
|
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
|
part |
part352 |
2010-06-01 |
|
|
ReCreate Foundation
Octinoxate, Octisalate, and Oxybenzone CREAM
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:51060-003 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
2.2125 mL
|
|
OCTISALATE OCTISALATE |
|
1.18 mL
|
|
OXYBENZONE OXYBENZONE |
|
.59 mL
|
Product Characteristics
|
|
Color
|
|
BROWN |
|
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
|
29.5 in 1 BOTTLE, PUMP |
|
|
|
2 |
NDC:51060-003-29 |
1 in 1 CARTON |
|
|
Marketing Information
|
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
|
part |
part352 |
2010-06-01 |
|
|
ReCreate Foundation
Octinoxate, Octisalate, and Oxybenzone CREAM
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:51060-004 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
2.2125 mL
|
|
OCTISALATE OCTISALATE |
|
1.18 mL
|
|
OXYBENZONE OXYBENZONE |
|
.59 mL
|
Product Characteristics
|
|
Color
|
|
BROWN |
|
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
|
29.5 in 1 BOTTLE, PUMP |
|
|
|
2 |
NDC:51060-004-29 |
1 in 1 CARTON |
|
|
Marketing Information
|
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
|
part |
part352 |
2010-06-01 |
|
|
ReCreate Foundation
Octinoxate, Octisalate, and Oxybenzone CREAM
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:51060-005 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
2.2125 mL
|
|
OCTISALATE OCTISALATE |
|
1.18 mL
|
|
OXYBENZONE OXYBENZONE |
|
.59 mL
|
Product Characteristics
|
|
Color
|
|
BROWN |
|
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
|
29.5 in 1 BOTTLE, PUMP |
|
|
|
2 |
NDC:51060-005-29 |
1 in 1 CARTON |
|
|
Marketing Information
|
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
|
part |
part352 |
2010-06-01 |
|
|
ReCreate Foundation
Octinoxate, Octisalate, and Oxybenzone CREAM
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:51060-006 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
2.2125 mL
|
|
OCTISALATE OCTISALATE |
|
1.18 mL
|
|
OXYBENZONE OXYBENZONE |
|
.59 mL
|
Product Characteristics
|
|
Color
|
|
BROWN |
|
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
|
29.5 in 1 BOTTLE, PUMP |
|
|
|
2 |
NDC:51060-006-29 |
1 in 1 CARTON |
|
|
Marketing Information
|
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
|
part |
part352 |
2010-06-01 |
|
|
ReCreate Foundation
Octinoxate, Octisalate, and Oxybenzone CREAM
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:51060-007 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
2.2125 mL
|
|
OCTISALATE OCTISALATE |
|
1.18 mL
|
|
OXYBENZONE OXYBENZONE |
|
.59 mL
|
Product Characteristics
|
|
Color
|
|
BROWN |
|
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
|
29.5 in 1 BOTTLE, PUMP |
|
|
|
2 |
NDC:51060-007-29 |
1 in 1 CARTON |
|
|
Marketing Information
|
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
|
part |
part352 |
2010-06-01 |
|
|
ReCreate Foundation
Octinoxate, Octisalate, and Oxybenzone CREAM
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:51060-008 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
2.2125 mL
|
|
OCTISALATE OCTISALATE |
|
1.18 mL
|
|
OXYBENZONE OXYBENZONE |
|
.59 mL
|
Product Characteristics
|
|
Color
|
|
BROWN |
|
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
|
29.5 in 1 BOTTLE, PUMP |
|
|
|
2 |
NDC:51060-008-29 |
1 in 1 CARTON |
|
|
Marketing Information
|
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
|
part |
part352 |
2010-06-01 |
|
|
ReCreate Foundation
Octinoxate, Octisalate, and Oxybenzone CREAM
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:51060-009 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
2.2125 mL
|
|
OCTISALATE OCTISALATE |
|
1.18 mL
|
|
OXYBENZONE OXYBENZONE |
|
.59 mL
|
Product Characteristics
|
|
Color
|
|
BROWN |
|
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
|
29.5 in 1 BOTTLE, PUMP |
|
|
|
2 |
NDC:51060-009-29 |
1 in 1 CARTON |
|
|
Marketing Information
|
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
|
part |
part352 |
2010-06-01 |
|
|
ReCreate Foundation
Octinoxate, Octisalate, and Oxybenzone CREAM
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:51060-010 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
2.2125 mL
|
|
OCTISALATE OCTISALATE |
|
1.18 mL
|
|
OXYBENZONE OXYBENZONE |
|
.59 mL
|
Product Characteristics
|
|
Color
|
|
BROWN |
|
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
|
29.5 in 1 BOTTLE, PUMP |
|
|
|
2 |
NDC:51060-010-29 |
1 in 1 CARTON |
|
|
Marketing Information
|
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
|
part |
part352 |
2010-06-01 |
|
|
ReCreate Foundation
Octinoxate, Octisalate, and Oxybenzone CREAM
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:51060-011 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
2.2125 mL
|
|
OCTISALATE OCTISALATE |
|
1.18 mL
|
|
OXYBENZONE OXYBENZONE |
|
.59 mL
|
Product Characteristics
|
|
Color
|
|
BROWN |
|
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
|
29.5 in 1 BOTTLE, PUMP |
|
|
|
2 |
NDC:51060-011-29 |
1 in 1 CARTON |
|
|
Marketing Information
|
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
|
part |
part352 |
2010-06-01 |
|
|
ReCreate Foundation
Octinoxate, Octisalate, and Oxybenzone CREAM
Product Information
|
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:51060-012 |
|
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Active Ingredient/Active Moiety
|
|
Ingredient Name
|
Basis of Strength
|
Strength
|
|
OCTINOXATE OCTINOXATE |
|
2.2125 mL
|
|
OCTISALATE OCTISALATE |
|
1.18 mL
|
|
OXYBENZONE OXYBENZONE |
|
.59 mL
|
Product Characteristics
|
|
Color
|
|
BROWN |
|
|
Packaging
|
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
|
1 |
|
29.5 in 1 BOTTLE, PUMP |
|
|
|
2 |
NDC:51060-012-29 |
1 in 1 CARTON |
|
|
Marketing Information
|
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
|
part |
part352 |
2010-06-01 |
|
|
