FDA.reportPublic FDA data

VSHELL SUNSCREEN

Manufacturer
Guangdong Miaolian Cosmetics Co., Ltd.
Effective date
2024-07-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:15:56

Label at a glance#

ProductVSHELL SUNSCREEN
Active ingredientZINC OXIDE
Label structure14 sections

Dosage and administration

Apply liberally and evenly 15 minutes prior to sun exposure.Reapply after 40 minutes of swimming or sweating immediately aftertowel drying "at least every 2 hours.

Storage and handling

Protect this product from excessive heat and direct sun.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 16%

Purpose

OTC - PURPOSE SECTION

Helps prevent sunburn

Use

INDICATIONS & USAGE SECTION

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 SECTION

For external use only

Do Not Use

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

When Using

OTC - WHEN USING SECTION

When using this product keep out of eyes.
Rinse with wate to remove.
Stop use and ask doctor if rash occurs.

Stop Use

OTC - STOP USE SECTION

Stop use and ask doctor if rash occurs

Ask Doctor

OTC - ASK DOCTOR SECTION

Not for use in children under 6 months old

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Iiswallowed, get medical help orcontact Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply liberally and evenly 15 minutes prior to sun exposure.Reapply after 40 minutes of swimming or sweating immediately aftertowel drying "at least every 2 hours.

Other information

STORAGE AND HANDLING SECTION

Protect this product from excessive heat and direct sun.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, C12-15 Alkyl Benzoate, Caprylic/Capric Triglyceride, Glyceryl Stearate, Helianthus Annuus (Sunflower) Seed Oil, Ricinus Communis (Castor) Seed Oil, Beeswax, Oryza Sativa (Rice) Bran Wax, Sorbitan Sesquioleate, Glycerin, Cetyl Alcohol, Stearyl Alcohol, Magnesium Aluminum Silicate, Butyrospermum Parkii (Shea) Butter, Camellia Sinensis Flower Extract, Ilex Paraguariensis Leaf Extract, Rosa Canina Fruit Oil, Tocopheryl Acetate, Carthamus Tinctorius (Safflower) Seed Oil, Rubus Idaeus (Raspberry) Fruit Extract, Squalane, Xanthan Gum, Propanediol, Ethylhexylglycerin, Potassium Sorbate, Fragrance

Questions

OTC - QUESTIONS SECTION

Call us！（0086）020-37411701

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VSHELL Sunscreen LabelVSHELL Sunscreen Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84507-006-012026-01-29C16284748780-149896155-a337-586f-e063-e6dba90add901df5ca5b-2ffd-6d5d-e063-6394a90af4c5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84507-006-01VSHELL SUNSCREEN50 g in 1 BOTTLECREAM502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84507-006VSHELL SUNSCREEN (SUNSCREEN) CREAM [GUANGDONG MIAOLIAN COSMETICS CO., LTD.]21 package rows20240725_1df5ca5b-2ffd-6d5d-e063-6394a90af4c5.zip

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84507-00684507-006-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

Name, UNII, Kind table
NameUNIIKind
SHEA BUTTERK49155WL9YIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
PROPANEDIOL5965N8W85TIACT
CASTOR OILD5340Y2I9GIACT
SORBITAN SESQUIOLEATE0W8RRI5W5AIACT
CETYL ALCOHOL936JST6JCNIACT
GLYCERINPDC6A3C0OXIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
STEARYL ALCOHOL2KR89I4H1YIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
ALLYL BENZOATEAQY5543KFEIACT
SQUALANEGW89575KF9IACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
MAGNESIUM ALUMINUM SILICATE6M3P64V0NCIACT
FRAGRANCE 135765EM498GW35IACT
ILEX PARAGUARIENSIS LEAF1Q953B4O4FIACT
SUNFLOWER OIL3W1JG795YIIACT
ROSA CANINA FRUIT OILCR7307M3QZIACT
CAMELLIA SINENSIS FLOWER9I2BJY2J17IACT
YELLOW WAX2ZA36H0S2VIACT
XANTHAN GUMTTV12P4NEEIACT
ALOE VERA LEAFZY81Z83H0XIACT
RASPBERRY4N14V5R27WIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
SAFFLOWER SEED8FCL6A31TXIACT
RICE BRANR60QEP13ICIACT
ZINC OXIDESOI2LOH54ZACTIB

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
1df855c0-53ec-2417-e063-6294a90a56551df5ca5b-2ffd-6d5d-e063-6394a90af4c52024-07-24WarningsExact identifier
spl id: 1df855c0-53ec-2417-e063-6294a90a5655
spl set id: 1df5ca5b-2ffd-6d5d-e063-6394a90af4c5

Reported adverse events (FAERS/openFDA)#

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