PERFECTING LIQUID FOUNDATION GOLDEN BRONZE SPF 15- zinc oxide emulsion

Perfecting Liquid Foundation Golden Bronze by

Drug Labeling and Warnings

Perfecting Liquid Foundation Golden Bronze 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, Polymethylsilsesquioxane, Glycerin, HDI/Trimethylol Hexyllactone Crosspolymer, Propanediol, Dimethicone, Hydrogenated Castor Oil, Phenoxyethanol, Magnesium Sulfate, Ribose, Sodium Chloride, Avena Sativa (Oat) Kernel Extract, Ethylhexylglycerin, Sodium Benzoate, Tocopheryl Acetate, Camellia Sinensis (White Tea) Leaf Extract, Caprylic/Capric Triglyceride, Potassium Sorbate, Aminobutyric Acid, Sodium Hyaluronate, Tetrahexyldecyl Ascorbate, Alaria Esculenta Extract, Buddleja Davidii Extract, Marrubium Vulgare Extract, Thymus Vulgaris (Thyme) Extract, Caprylyl Glycol.

May Contain: Titanium Dioxide (CI 77891), Iron Oxide (CI 77492), Iron Oxides (CI 77491), Iron Oxides (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.

INDICATIONS & USAGE

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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PERFECTING LIQUID FOUNDATION GOLDEN BRONZE  SPF 15
zinc oxide emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42508-476
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)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
ISODODECANE (UNII: A8289P68Y2)
HYDROGENATED POLYDECENE (1500 CST) (UNII: 4YI0729529)
POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
GLYCERIN (UNII: PDC6A3C0OX)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PROPANEDIOL (UNII: 5965N8W85T)
DIMETHICONE (UNII: 92RU3N3Y1O)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
RIBOSE, D- (UNII: 681HV46001)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
OAT (UNII: Z6J799EAJK)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SODIUM BENZOATE (UNII: OJ245FE5EU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
.GAMMA.-AMINOBUTYRIC ACID (UNII: 2ACZ6IPC6I)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
ALARIA ESCULENTA (UNII: EJ9JK8J58D)
BUDDLEJA DAVIDII WHOLE (UNII: 8JZ8B2V1OV)
MARRUBIUM VULGARE WHOLE (UNII: 7A72MUN24Z)
THYMUS VULGARIS WHOLE (UNII: 8L72OKJ7II)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42508-476-01	1 in 1 CARTON	06/30/2021
1		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 Drug	M020	06/30/2021

Labeler - Arbonne International, LLC (961643454)