FDA.reportPublic FDA data

Pure Velocity SUNSCREEN SPF30

Manufacturer
Guangzhou Haishi Biological Technology Co., Ltd.
Effective date
2025-09-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:15:17

Label at a glance#

ProductPure Velocity SUNSCREEN SPF30
Active ingredientETHYLHEXYL METHOXYCINNAMATE, HOMOSALATE, OCTOCRYLENE
Label structure11 sections

Indications and uses

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.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

OCTOCRYLENE 4%
HOMOSALATE 2.5%
ETHYLHEXYL METHOXYCINNAMATE 2%

Purpose

OTC - PURPOSE SECTION

SUNSCREEN

Uses

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

Stop Use

OTC - STOP USE SECTION

Rinse with wate to remove.
Stop use and ask doctor if rash occurs.

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.

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out Of Reach Of Children

Dosage & administration

DOSAGE & ADMINISTRATION SECTION

Squeeze out an appropriate amount of Sunscreen and spread evenly on skin.

Inactive ingredients

INACTIVE INGREDIENT SECTION

CYCLOPENTASILOXANE 15%

CYCLOHEXASILOXANE 7.5%

ETHYLHEXYL PALMITATE 6%

OZOKERITE 2.5%

MICROCRYSTALLINE WAX 2.5%

DICAPRYLYL CARBONATE 3%

THEOBROMA CACAO (COCOA) SEED BUTTER 2%

SILICA 1%

POLYMETHYLSILSESQUIOXANE 3%

CERAMIDE NP 0.5%

POLYGLYCERYL-2 TRIISOSTEARATE 1%

BISABOLOL 0.1%

TOCOPHEROL 0.2%

PHENOXYETHANOL 0.35%

AROMA 0.3%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label.Label.

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60771-0030-1Pure Velocity SUNSCREEN SPF3015 g in 1 TUBESTICK151

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60771-003060771-0030-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
CYCLOPENTASILOXANE0THT5PCI0RIACT
MICROCRYSTALLINE WAXXOF597Q3KYIACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
POLYMETHYLSILSESQUIOXANE (11 MICRONS)Z570VEV8XKIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYL METHOXYCINNAMATE4Y5P7MUD51ACTIB
ETHYLHEXYL PALMITATE2865993309IACT
POLYGLYCERYL-2 TRIISOSTEARATE68DUY2D39AIACT
PARFUMIDINEA2Q2LHC6MAIACT
BEESWAX2ZA36H0S2VIACT
HOMOSALATEV06SV4M95SACTIB
CERAMIDE NP4370DF050BIACT
OCTOCRYLENE5A68WGF6WMACTIB
CYCLOHEXASILOXANEXHK3U310BAIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
TOCOPHEROLR0ZB2556P8IACT
BISABOLOL24WE03BX2TIACT
THEOBROMA CACAO (COCOA) SEED BUTTER512OYT1CRRIACT

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
5ab95f88-667b-3241-e063-6394a90ab73d4000a5b9-e7a3-b5d3-e063-6294a90a25062026-09-05WarningsExact identifier
spl set id: 4000a5b9-e7a3-b5d3-e063-6294a90a2506

Reported adverse events (FAERS/openFDA)#

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