SPF 25 Finishing Powder

Manufacturer
Younique LLC | Oxygen Development, LLC
Effective date
2018-10-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:57:02

Label at a glance#

ProductSPF 25 Finishing Powder
Label structure8 sections

Indications and uses

Apply generously 15 minutes before sun exposure. Reapply immediately after towel drying. Reapply at least every 2 hours. Helps prevent sunburn. If used as directed with other sun protection measures decreases the risk of skin cancer and early skin aging caused by the sun.

Dosage and administration

Apply generously 15 minutes before sun exposure. Reapply immediately after towel drying. Reapply at least every 2 hours.

Label contents#

Full prescribing information#

Directions

DOSAGE & ADMINISTRATION SECTION

Apply generously 15 minutes before sun exposure.

Reapply immediately after towel drying.

Reapply at least every 2 hours.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Polymethylsilsesquioxane, Silica, Jojoba Esters, Alumina, Oryza Sativa (Rice) Extract, Caprylyl Glycol, Phenoxyethanol, Hexylene Glycol, Aluminum Dimyristate, Triethoxycaprylylsilane, Disodium Stearoyl Glutamate, Iron Oxides, Mica.

Directions & Uses

INDICATIONS & USAGE SECTION

Apply generously 15 minutes before sun exposure.

Reapply immediately after towel drying.

Reapply at least every 2 hours.

Helps prevent sunburn.

If used as directed with other sun protection measures decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Purpose

OTC - PURPOSE SECTION

Sunscreen.

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 15%

Zinc Oxide 17%

Warnings

WARNINGS SECTION

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 Posion Control Center right away

Package.Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71182-1706-42020-01-31C16284748780-19d75b9d0-0bb6-f424-e053-dadaa90a57ceSPF 25 Finishing Powder

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71182-1706-4SPF 25 Finishing Powder4 g in 1 JARPOWDER42
71182-1706-4SPF 25 Finishing Powder1 in 1 CARTONPOWDER12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71182-1706SPF 25 FINISHING POWDER (ZINC OXIDE, TITANIUM DIOXIDE) POWDER [YOUNIQUE LLC]22 package rows20181017_77e777c1-748b-a48d-e053-2991aa0ac280.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71182-170671182-1706-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
77e777c1-748c-a48d-e053-2991aa0ac28077e777c1-748b-a48d-e053-2991aa0ac2802018-10-12WarningsExact identifier
spl id: 77e777c1-748c-a48d-e053-2991aa0ac280
spl set id: 77e777c1-748b-a48d-e053-2991aa0ac280

Reported adverse events (FAERS/openFDA)#

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