FDA.reportPublic FDA data

Pure velocity SUNSCREEN SPF 50

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 01:15:18

Label at a glance#

ProductPure velocity SUNSCREEN SPF 50
Active ingredientETHYLHEXYL METHOXYCINNAMATE, ZINC OXIDE
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

ETHYLHEXYL METHOXYCINNAMATE

ZINC OXIDE

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

WATER

PETROLATUM

ISOPROPYL PALMITATE

CETEARYL GLUCOSIDE

POLYDIMETHYLSILOXANE

HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER

POLYISOBUTYLENE

PEG-7 TRIMETHYLOLPROPANE COCONUT ETHER

SODIUM HYALURONATE

TOCOPHERYL ACETATE

POLYETHER-1

CITRIC ACID

OLEANOL POLYETHER-3 PHOSPHATE

PHENOXYETHANOL

BUTANEDIOL

IODOPROPYNYL BUTYLCARBAMATE

TRIETHOXYOCTYLSILANE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label.Label.

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60771-0031-1Pure velocity SUNSCREEN SPF 5030 g in 1 BOTTLELIQUID301

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
60771-003160771-0031-1

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
PETROLATUM4T6H12BN9UIACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)86FQE96TZ4IACT
PEG-7 TRIMETHYLOLPROPANE COCONUT ETHERMVJ3AD73GGIACT
ISOPROPYL PALMITATE8CRQ2TH63MIACT
POLYETHER-1 (2800 MPA.S)6QR7NJP3G8IACT
.ALPHA.-BUTYLDIMETHYLSILYL-AND .OMEGA.-3-METHACRYLOXYPROPYLDIMETHYLSILYL-TERMINATED POLYDIMETHYLSILOXANE (10000 MW)P7CQ6Y7QTSIACT
CITRIC ACID2968PHW8QPIACT
ETHYLHEXYL METHOXYCINNAMATE4Y5P7MUD51ACTIB
ZINC OXIDESOI2LOH54ZACTIB
WATER059QF0KO0RIACT
POLYISOBUTYLENE (1000 MW)5XB3A63Y52IACT
SODIUM HYALURONATEYSE9PPT4THIACT
1,2-BUTANEDIOLRUN0H01QEUIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
CETEARYL GLUCOSIDE09FUA47KNAIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
PHENOXYETHANOLHIE492ZZ3TIACT

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
5ab96d0a-d016-40f0-e063-6394a90aa80840024b26-6117-7bae-e063-6294a90a33eb2026-09-05WarningsExact identifier
spl set id: 40024b26-6117-7bae-e063-6294a90a33eb

Reported adverse events (FAERS/openFDA)#

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