Perfecting Liquid Foundation Deep Bronze

Manufacturer
Arbonne International, LLC
Effective date
2022-12-09
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:44:52

Label at a glance#

ProductPerfecting Liquid Foundation Deep Bronze SPF 15
Active ingredientZINC OXIDE
Label structure9 sections

Dosage and administration

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 inc...

Storage and handling

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

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients      Purpose

Zinc Oxide 10 %               Sunscreen

OTC - PURPOSE SECTION

Enter section text here

INSTRUCTIONS FOR USE SECTION

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 SECTION

Warnings
For external use only

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - WHEN USING SECTION

When using this product keep out of eyes.  Rinse with water to remove.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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 SECTION


Other information

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

INACTIVE INGREDIENT SECTION

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)

OTC - QUESTIONS SECTION

Questions of comments?

1.800.272.6663

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

HOW SUPPLIED SECTION

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

Made in the U.S.A.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PerfectingUCPerfectingUC

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42508-47342508-473-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 35 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ef68546c-3503-3d64-e053-2a95a90aad174fcb101c-4d87-4e3a-be87-e6810a0b315e2022-12-09WarningsExact identifier
spl id: ef68546c-3503-3d64-e053-2a95a90aad17
spl set id: 4fcb101c-4d87-4e3a-be87-e6810a0b315e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.