PURE VELOCITY SUNSCREEN SPF 50- ethylhexyl methoxycinnamate,zinc oxide liquid

Pure velocity SUNSCREEN SPF 50 by

Drug Labeling and Warnings

Pure velocity SUNSCREEN SPF 50 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

ETHYLHEXYL METHOXYCINNAMATE

ZINC OXIDE

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

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PURE VELOCITY SUNSCREEN SPF 50 
ethylhexyl methoxycinnamate,zinc oxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60771-0031
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ETHYLHEXYL METHOXYCINNAMATE (UNII: 4Y5P7MUD51) (ETHYLHEXYL METHOXYCINNAMATE - UNII:4Y5P7MUD51)	ETHYLHEXYL METHOXYCINNAMATE	1.5 g  in 100 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PETROLATUM (UNII: 4T6H12BN9U)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
PEG-7 TRIMETHYLOLPROPANE COCONUT ETHER (UNII: MVJ3AD73GG)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
POLYETHER-1 (2800 MPA.S) (UNII: 6QR7NJP3G8)
.ALPHA.-BUTYLDIMETHYLSILYL-AND .OMEGA.-3-METHACRYLOXYPROPYLDIMETHYLSILYL-TERMINATED POLYDIMETHYLSILOXANE (10000 MW) (UNII: P7CQ6Y7QTS)
CITRIC ACID (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)
POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
1,2-BUTANEDIOL (UNII: RUN0H01QEU)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60771-0031-1	30 g in 1 BOTTLE; 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(60771-0031)