PURE VELOCITY SUNSCREEN SPF30- octocrylene,homosalate,ethylhexyl methoxycinnamate stick

Pure Velocity SUNSCREEN SPF30 by

Drug Labeling and Warnings

Pure Velocity SUNSCREEN SPF30 by is a Otc medication manufactured, distributed, or labeled by Guangzhou Haishi Biological Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

OCTOCRYLENE 4%
HOMOSALATE 2.5%
ETHYLHEXYL METHOXYCINNAMATE 2%

Purpose

SUNSCREEN

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.

Warnings

For external use only

Stop Use

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

Do Not Use

Do not use on damaged or broken skin.

When Using

When using this product keep out of eyes.

Keep Out Of Reach Of Children

Keep Out Of Reach Of Children

Dosage & administration

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

Inactive ingredients

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%

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PURE VELOCITY SUNSCREEN SPF30 
octocrylene,homosalate,ethylhexyl methoxycinnamate stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60771-0030
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ETHYLHEXYL METHOXYCINNAMATE (UNII: 4Y5P7MUD51) (ETHYLHEXYL METHOXYCINNAMATE - UNII:4Y5P7MUD51)	ETHYLHEXYL METHOXYCINNAMATE	2 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	2.5 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CYCLOPENTASILOXANE (UNII: 0THT5PCI0R)
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
POLYGLYCERYL-2 TRIISOSTEARATE (UNII: 68DUY2D39A)
PARFUMIDINE (UNII: A2Q2LHC6MA)
BEESWAX (UNII: 2ZA36H0S2V)
CERAMIDE NP (UNII: 4370DF050B)
CYCLOHEXASILOXANE (UNII: XHK3U310BA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
TOCOPHEROL (UNII: R0ZB2556P8)
BISABOLOL (UNII: 24WE03BX2T)
THEOBROMA CACAO (COCOA) SEED BUTTER (UNII: 512OYT1CRR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60771-0030-1	15 g in 1 TUBE; Type 0: Not a Combination Product	09/30/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	09/30/2025

Labeler - Guangzhou Haishi Biological Technology Co., Ltd. (421262738)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Haishi Biological Technology Co., Ltd.		421262738	manufacture(60771-0030)