FDA.reportPublic FDA data

VGO UV Clear Sunscreen

Manufacturer
Beaupan USA,Inc.
Effective date
2025-05-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:39:08

Label at a glance#

ProductVGO UV Clear Sunscreen
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

ADVERSE REACTIONS SECTION

ZINC OXIDE 5%

OTC - PURPOSE SECTION

Helps prevent sunburn

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

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.

INACTIVE INGREDIENT SECTION

WATER, GLYCERIN, CYCLOPENTASILOXANE, ISOHEXADECANE, BIS-PEG-18 METHYL ETHER DIMETHYL SILANE, SORBETH-30 TETRAOLEATE, AMMONIUM POLYACRYLOYLDIMETHYL TAURATE, PEG/PPG-14/7 DIMETHYL ETHER, SODIÚM POLYACRYLATE, PEG-10 DIMETHICONE, POLYHYDROXYSTEARIC ACID, ETHYLHEXYL STEARATE, PHENOXYETHANOL, POTASSIUM CETYL PHOSPHATE, METHYLPARABEN,TRIETHOXYCAPRYLYLSILANE, SILICA, GLYCINE SOJA (SOYBEAN) SEED EXTRACT, TRIDECETH-6, LACTIC ACID, FRAGRANCE, ETHYLHEXYLGLYCERIN,ΕΤΗΚΥHΕXΚY ΜΕΤHOXYCINNAMATE.

INDICATIONS & USAGE SECTION

apply generously 15 minutes before sun exposure and as needed.

reapply at least every 2 hours. use a water-resistant sunscreen if swimming or sweating.

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 sun exposure.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

UV Clear SunscreenUV Clear Sunscreen

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85530-251VGO UV CLEAR SUNSCREEN (ZINC OXIDE 5%) CREAM [BEAUPAN USA,INC.]1Unmatched20250512_34c699a1-56f4-ff0e-e063-6394a90afa8c.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85530-25185530-251-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
TRIDECETH-63T5PCR2H0CIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
ZINC OXIDESOI2LOH54ZACTIB
WATER059QF0KO0RIACT
AMMONIUM POLYACRYLOYLDIMETHYL TAURATEF01RIY4371IACT
METHYLPARABENA2I8C7HI9TIACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
BIS-PEG-18 METHYL ETHER DIMETHYL SILANEOEB4R3WW9CIACT
PHENOXYETHANOLHIE492ZZ3TIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
POTASSIUM CETYL PHOSPHATE03KCY6P7UTIACT
ISOHEXADECANE918X1OUF1EIACT
GLYCERINPDC6A3C0OXIACT
ETHYLHEXYL STEARATEEG3PA2K3K5IACT
SORBETH-30 TETRAOLEATE5KSN7B8P6PIACT
LACTIC ACID33X04XA5ATIACT
PEG/PPG-14/7 DIMETHYL ETHER6DNW9T7YT2IACT

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
3fcaacaa-3946-7f48-e063-6394a90a0f9d34c699a1-56f4-ff0e-e063-6394a90afa8c2025-09-27Warnings, Adverse reactionsExact identifier
spl set id: 34c699a1-56f4-ff0e-e063-6394a90afa8c

Reported adverse events (FAERS/openFDA)#

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