FDA.reportPublic FDA data

Pure velocity TINTED SUNSCREEN SPF 50

Manufacturer
Guangdong Aimu Biological Technology Co., Ltd | 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 TINTED SUNSCREEN SPF 50
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
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

ZINC OXIDE
TITANIUM DIOXIDE

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
GLYCEROL
PROPYLENE GLYCOL
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL
POLYGLYCERYL-2 TRIISOSTEARATE
PHENYL TRIMETHICONE
DICAPRYLYL CARBONATE
ETHYLHEXYL METHOXYCINNAMATE
TRIMETHYLSILOXYSILICATE
CERA ALBA
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER
BENTONITE
SODIUM CHLORIDE
ASCORBIC ACID POLYPEPTIDE
CERAMIDE NP
SPHINGOMONAS FERMENT EXTRACT
SILICA
MAGNESIUM STEARATE
PEG-30 DIPOLYHYDROXYSTEARATE
XANTHAN GUM
SODIUM HYALURONATE
BISABOLOL
TOCOPHEROL
PHENOXYETHANOL
ETHYLHEXYLGLYCERIN
SOLANUM LYCOPERSICUM (TOMATO) FRUIT EXTRACT
TREMELLA FUCIFORMIS (MUSHROOM) EXTRACT
LILIUM CANDIDUM FLOWER EXTRACT
DENDROBIUM NOBILE EXTRACT
STEPHANIA TETRANDRA EXTRACT
TARAXACUM OFFICINALE (DANDELION) LEAF EXTRACT
SAURURUS CHINENSIS LEAF/ROOT EXTRACT
CI 77492
CI 77491
CI 77499
PARFUM

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label.Label.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60771-0035-1Pure velocity TINTED SUNSCREEN SPF 5050 g in 1 BOTTLECREAM501

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60771-003560771-0035-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
ASCORBIC ACIDPQ6CK8PD0RIACT
SODIUM CHLORIDE451W47IQ8XIACT
DIMETHICONOL/TRIMETHYLSILOXYSILICATE CROSSPOLYMER (35/65 W/W; 10000000 PA.S)TEU31AO9BNIACT
DIPROPYLENE GLYCOL CAPRYLATECJ981S4H3TIACT
POLYGLYCERYL-2 TRIISOSTEARATE68DUY2D39AIACT
PHENYL TRIMETHICONEDR0K5NOJ4RIACT
ABIES PROCERA LEAFJ2Y55K311IIACT
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE)H895X08VNQIACT
MAGNESIUM STEARATE70097M6I30IACT
ZINC OXIDESOI2LOH54ZACTIB
DICAPRYLYL CARBONATE609A3V1SUAIACT
WATER059QF0KO0RIACT
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL724GKU717MIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
DIPALMITOYLPHOSPHATIDYLGLYCEROL, DL-VA9U6BR3SBIACT
BENTONITEA3N5ZCN45CIACT
ALUMINUM HEXAFLUOROSILICATEE7I96VX9N6IACT
CERAMIDE NP4370DF050BIACT
LIMOSILACTOBACILLUS FERMENTUM2C1F12C6APIACT

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
5ab994ec-a54c-061a-e063-6294a90a2ca240049f9d-7057-05c2-e063-6294a90acbba2026-09-05WarningsExact identifier
spl set id: 40049f9d-7057-05c2-e063-6294a90acbba

Reported adverse events (FAERS/openFDA)#

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