Face Sunscreen

Manufacturer
Shenzhen Rushen E-commerce Co.. Ltd.
Effective date
2024-06-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:14:31

Label at a glance#

ProductFace Sunscreen
Active ingredientOCTINOXATE, ZINC OXIDE
Label structure13 sections

Indications and uses

Apply sunscreen generously to exposedskin. Rub it in evenly. Reapply as neededespecially after swimming or sweating.Enjoy your sun-protected day!

Storage and handling

Other information Before use, read all information on thecarton Store at controlled room temperature20 to 25 C (68 to 77°F)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 9.0%
Octinoxate 7.5%

OTC - PURPOSE SECTION

Sunscreen
Moisturizes throughout theday & helps protects

Uses

INDICATIONS & USAGE SECTION

Apply sunscreen generously to exposedskin. Rub it in evenly. Reapply as neededespecially after swimming or sweating.Enjoy your sun-protected day!

Wamings

WARNINGS SECTION

For exteral use only

DESCRIPTION SECTION

Do not use
on damaged or broken skin

OTC - WHEN USING SECTION

When using this product
Only for external use. do not ingest.
Avoid direct contact with eyes.

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.

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask Doctor
When Pregnant or breast-feeding.

DOSAGE & ADMINISTRATION SECTION

Directions
Directions for use
-apply liberally 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 B road.
-Spectrum SPF value of15 or higher and other sun protection:
-limit time in the sun, especially from 10 a.m.-2 p.m.
-and wear long-sleeved shirts, pants, hats, and sunglasses

STORAGE AND HANDLING SECTION

Other information
Before use, read all information on thecarton Store at controlled room temperature20 to 25 C (68 to 77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Cetearyl Alcohol, Butylene Glycol,Niacinamide, Sodium Hyaluronate, Tocopherol, Centella,Asiatica Extract,Camellia Sinensis Leaf Extract,Ethylhexylglycerin, Carbomer, Triethoxycaprylyisilane,Phenoxyethanol,Xanthan Gum,Additional Ingredients(Fragrances,Stabilizers,etc.),Dibutyl Adipate,Polymethylsiisesquioxane,Coco-Caprylate/Caprate,Hyalur

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84431-001-012025-07-29C16284748780-13b156c62-2766-fb37-e063-e6dba90a4e071b392fcd-46ee-6715-e063-6394a90a9c3d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84431-001-01Face Sunscreen50 g in 1 BOTTLECREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84431-001FACE SUNSCREEN (SUNSCREEN) CREAM [SHENZHEN RUSHEN E-COMMERCE CO.. LTD.]11 package rows20240701_1b392fcd-46ee-6715-e063-6394a90a9c3d.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84431-00184431-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
1b392fcd-46ef-6715-e063-6394a90a9c3d1b392fcd-46ee-6715-e063-6394a90a9c3d2024-06-19WarningsExact identifier
spl id: 1b392fcd-46ef-6715-e063-6394a90a9c3d
spl set id: 1b392fcd-46ee-6715-e063-6394a90a9c3d

Reported adverse events (FAERS/openFDA)#

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