PERFECTING LIQUID FOUNDATION NEUTRAL BEIGE SPF 15- zinc oxide emulsion

Perfecting Liquid Foundation Neutral Beige by

Drug Labeling and Warnings

Perfecting Liquid Foundation Neutral Beige by is a Otc medication manufactured, distributed, or labeled by Arbonne International, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients      Purpose

Zinc Oxide 10 %               Sunscreen

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INSTRUCTIONS FOR USE

Uses  

• helps prevent sunburn   
  
• if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

WARNINGS

Warnings
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

For sunscreen use:

• apply liberally and evenly 15 minutes before sun exposure
• reapply at least every 2 hours
• use a water resistant sunscreen if swimming or sweating
• Sun Protection Measures

            Spending time in the sun increases your risk of skin cancer and early skin aging.  To decrease this risk, regularly use a sunscreen with a broad spectrum SPF                     value of 15 or higher and other sun protection measures including:

• limit time in the sun, especially from 10 a.m.-2 p.m.
• wear long-sleeved shirts, pants, hats, and sunglasses.
• Children under 6 months of age: Ask a doctor.

STORAGE AND HANDLING

Other information

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

INACTIVE INGREDIENT

Inactive ingredients   water, cyclopentasiloxane, isododecane, hydrogenated polydecene, polyglyceryl-3 diisostearate, polymethylsilsequioxane, glycerin,  HDI/trimethylol hexyllactone crosspolymer,  propanediol, dimethicone, hydrogenated castor oil, magnesium sulfate, ribose, avena sativa (oat) kernael extract, camellia sinensis leaf extract, alaria esculenta extract, buddleja davidii extract, thymus vulgaris (thyme) extract, maruubium vulgare extract, hexapeptide-10, tocopheryl acetate, retinyl palmitate, tetrahexyldecyl ascorbate, aminobutyric acid, caprylic/capric triglyceride, sodium hyaluronate, sodium chloride, ethylhexylglycerin, caprylyl glycol, phenoxyethanol, sodium benzoate, potassium sorbate. May Contain:  titanium dioxide (CI 77891), iron oxides (CI 77491, CI77492, CI 77499).

QUESTIONS

Questions of comments?

1.800.272.6663

Monday - Friday 6 a.m. - 6 p.m. Pacific Time.

HOW SUPPLIED

Distributed by Arbonne International, LLC.   Irvine, CA 92618  U.S.A

Made in the U.S.A.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PERFECTING LIQUID FOUNDATION NEUTRAL BEIGE  SPF 15
zinc oxide emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42508-159
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	10 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
THYME (UNII: CW657OBU4N)
MARRUBIUM VULGARE (UNII: 7A72MUN24Z)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
.GAMMA.-AMINOBUTYRIC ACID (UNII: 2ACZ6IPC6I)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
OAT (UNII: Z6J799EAJK)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ISODODECANE (UNII: A8289P68Y2)
DIMETHICONE (UNII: 92RU3N3Y1O)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42508-159-02	1 in 1 CARTON	03/01/2010
1	NDC: 42508-159-01	30 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	03/01/2010

Labeler - Arbonne International, LLC (021541164)