FDA.reportPublic FDA data

VGO LIGHT AND CLEAR SUNSCREEN

Manufacturer
HainanShengtaizhuoInternationalInformationDevelopmentCo.,Ltd. | Hainan Shengtaizhuo International Information Development Co., LTD
Effective date
2024-06-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:58:39

Label at a glance#

ProductVGO LIGHT AND CLEAR SUNSCREEN
Active ingredientTITANIUM DIOXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

TITANIUM DIOXIDE

OTC - PURPOSE SECTION

Sunscreen

WARNINGS SECTION

For external use only.
Do not use on damaged or broken skin.
Stop use and ask a doctor if rash occurs.
When using this product keep out of eyes. Rinse with water to remove

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. 

INDICATIONS & USAGE SECTION

Apply liberally 15 minutes before sun exposure and
as needed.
• Reapply:
• After 40 minutes of swimming or sweating
• Immediately after towel drying
• At least every 2 hours
• Children under 6 months of age: ask a doctor.
• 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 your time in the sun, especially from 10 a.m. – 2 p.m.
• Wear long-sleeved shirts, pants, hats, and sunglasses.

INACTIVE INGREDIENT SECTION

ATER、DIMETHICONE、ISOHEXADECANE、GLYCERIN、BUTYLENE GLYCOL、PHENKYBENZIMIDAZOLE SULFONIC ACID、PEG-10 DIMETHICONE、SILICA、LAURYL PEG-10 TRIS(TRIMETHYLSILOXY)SILYLETHYL DIMETHICONE、DIISOSTEARKY MALATE、PENTAERYTHRITYL TETRAETHYLHEXANOATE、DISTEARDIMONIUM HECTORITE、ALUMINUM HYDROXIDE、SODIUM CHLORIDE、1,2-HEXANEDIOL、STEARIC ACID、POTASSIUM HYDROXIDE、NIACINAMIDE、PROPYLENE CARBONATE、HYDROXYACETOPHENONE、VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER、CI 77288、BUTYLENE GLYCOL、PENTYLENE GLYCOL、FRAGRANCE、HYDROXYPHENYL PROPAMIDOBENZOIC ACID、TRIETHOXYC/APRYLYLSILANE、ASCORBYL PALMITATE、TOCOPHEROL

DOSAGE & ADMINISTRATION 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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VGO LIGHT AND CLEAR SUNSCREEN LOTION

Reduce darkness and sunburn

Reduce darkness and sunburnReduce darkness and sunburn

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84556-269-012025-09-27C16284748780-13b156c62-24b7-fb37-e063-e6dba90a4e071a4934e3-9bfb-1921-e063-6294a90a9264
84556-269-012025-07-29C16284748780-13b156c62-24b7-fb37-e063-e6dba90a4e071a4934e3-9bfb-1921-e063-6294a90a9264

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84556-269VGO LIGHT AND CLEAR SUNSCREEN (TITANIUM DIOXIDE) LOTION [HAINANSHENGTAIZHUOINTERNATIONALINFORMATIONDEVELOPMENTCO.,LTD.]1Unmatched20240719_1a4934e3-9bfb-1921-e063-6294a90a9264.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84556-26984556-269-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHICONE92RU3N3Y1OIACT
NIACINAMIDE25X51I8RD4IACT
GLYCERINPDC6A3C0OXIACT
PEG-10 DIMETHICONE (500 CST)BR768L8A3TIACT
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER9NH1UDD2RRIACT
ISOHEXADECANE918X1OUF1EIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
PROPYLENE CARBONATE8D08K3S51EIACT
SODIUM CHLORIDE451W47IQ8XIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
PENTAERYTHRITYL TETRAETHYLHEXANOATEXJ7052W897IACT
1,2-HEXANEDIOLTR046Y3K1GIACT
POTASSIUM HYDROXIDEWZH3C48M4TIACT
HYDROXYPHENYL PROPAMIDOBENZOIC ACID25KRT26H77IACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT

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
3fca3bb5-4c0c-fb4b-e063-6394a90a46b41a4934e3-9bfb-1921-e063-6294a90a92642025-09-27WarningsExact identifier
spl set id: 1a4934e3-9bfb-1921-e063-6294a90a9264

Reported adverse events (FAERS/openFDA)#

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