Cream

Manufacturer
OXYGEN DEVELOPMENT, LLC
Effective date
2023-02-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:53:56

Label at a glance#

ProductCream
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure9 sections

Indications and 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.

Dosage and administration

Shake before use. Apply liberally 15 minutes before sun exposure. Use a water-resistant sunscreen of swimming or sweating. Reapply at least every 2 hours. Children under 6 months: Ask a doctor. Sun Protection Measures. Spending time in the sun increases our 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 protect...

Storage and handling

Shake before use. Apply liberally 15 minutes before sun exposure. Use a water-resistant sunscreen of swimming or sweating. Reapply at least every 2 hours. Children under 6 months: Ask a doctor. Sun Protection Measures. Spending time in the sun increases our 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 protect...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 4.55%

Zinc Oxide 3.5%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • 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 AND PRECAUTIONS SECTION

For external use only

OTC - STOP USE SECTION

Stop use and ask doctor if rash occurs.

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 - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

STORAGE AND HANDLING SECTION

  • Shake before use.
  • Apply liberally 15 minutes before sun exposure.
  • Use a water-resistant sunscreen of swimming or sweating.
  • Reapply at least every 2 hours.
  • Children under 6 months: Ask a doctor.
  • Sun Protection Measures. Spending time in the sun increases our 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.- 2p.m.

Wear long-sleeved shirts, pants, hats and sunglasses.

Other information

STORAGE AND HANDLING SECTION

  • Protect the product in this container from excessive heat and direct sunlight.
  • You may report a serious adverse reaction to: tarte c/o Report Reaction, LLC, P.O. Box 22, Plainsboro, NJ 08536-0222.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane, Isododecane, Polysilicone-11, Mica, Polymethylsilsesquioxane, Hexyl Laurate, PEG-10 Dimethicone, Polyglyceryl-4 Isostearate, Stearic Acid, Cetyl PEG/PPG-10/1 Dimethicone, Alumina, Triethoxycaprylylsilane, Dipalmitoyl Hydroxyproline, Diamond Powder, Iron Oxides.

Primary Package (Inner)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30 ML 61354-051-34 61354-051-34_AW61354-051-34_AW 61354-051-34_AW61354-051-34_AW

Secondary Package (Outer)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

61354-051-34_AW61354-051-34_AW30ml 61354-051-34

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61354-051-34Cream1 in 1 CARTONLOTION12
61354-051-34Cream30 mg in 1 TUBELOTION302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61354-051CREAM (TITANIUM DIOXIDE, ZINC OXIDE) LOTION [OXYGEN DEVELOPMENT, LLC]2Legacy NDC, 2 package rows20230211_bc3f8d67-8f4c-435f-e053-2995a90abda4.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61354-05161354-051-34

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
f45cf528-2bfb-ff03-e053-2a95a90ad530bc3f8d67-8f4c-435f-e053-2995a90abda42023-02-10WarningsExact identifier
spl id: f45cf528-2bfb-ff03-e053-2a95a90ad530
spl set id: bc3f8d67-8f4c-435f-e053-2995a90abda4

Reported adverse events (FAERS/openFDA)#

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