PHOFAY MATTE SUNSCREEN LIQUID FOUNDATION SPF 30 5- ensulizole,homosalate,octinoxate,titanium dioxide lotion

PHOFAY Matte Sunscreen Liquid Foundation SPF 30 5 by

Drug Labeling and Warnings

PHOFAY Matte Sunscreen Liquid Foundation SPF 30 5 by is a Otc medication manufactured, distributed, or labeled by Longway Technology(Guangzhou) Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ensulizole 2%,Homosalate 5%,Octinoxate 4.995%,Titanium Dioxide 10.725%

KEEP OUT OF REACH OF CHILDREN

if product is swallowed,get medical help or contact a poison control center right away.

WARNINGS

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes.

rinse with water to remove.

Stop Use And Ask A Doctor lf

rash or irritation develops and lasts

keep out of reach of children.

if product is swallowed,get medical help or contact a poison control center right away.

DOSAGE & ADMINISTRATION

For sunscreen use:
apply liberally 15 minutes before sun exposure

reapply at least every two hours

use a water resistant sunscreen if swimming or sweating

wear long-sleeved shirts, pants, hats and sunglasses

children under 6 months :Ask a doctor

INACTIVE INGREDIENT

Water,Glycerin, Silica, C12-15 Alkyl Benzoate, PhenylTrimethicone,Butylene Glycol, Cyclopentasiloxane,Polyglyceryl-3 Diisostearate, Sorbitan lsostearate, Tridecyl Trimellitate,Diisostearyl Malate,Polyglyceryl-2 Dipolyhydroxystearate, Phenoxyethanol,Triethoxycaprylylsilane,Disteardimonium Hectorite, Polyhydroxystearic Acid, Magnesium Sulfate, Sodium Chloride,Alumina,Sodium Hydroxide, Fragrance, Ethylhexylglycerin, BHT,lron Oxides(Cl77492,C177491,C177499)

OTHER SAFETY INFORMATION

protect the product in this container from excessive

heat and direct sun

PURPOSE

Suncreen

INDICATIONS & USAGE

helps prevent sunburn

provides high protection against sunburn and tanning

lf used as directed with other sun protection measures.

decreases the risk of skin cancer and early skin aging caused by the sun

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PHOFAY MATTE SUNSCREEN LIQUID FOUNDATION SPF 30 5 
ensulizole,homosalate,octinoxate,titanium dioxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85161-128
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	0.05 g  in 1 g
ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42)	ENSULIZOLE	0.02 g  in 1 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	0.10725 g  in 1 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	0.04995 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
CYCLOPENTASILOXANE (UNII: 0THT5PCI0R)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
CI 77492 (UNII: EX438O2MRT)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
ALUMINA (UNII: LMI26O6933)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
TRIDECYL TRIMELLITATE (UNII: FY36J270ES)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
WATER (UNII: 059QF0KO0R)
BHT (UNII: 1P9D0Z171K)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
FRAGRANCE LEMON ORC2001060 (UNII: K1725A7G95)
CI 77499 (UNII: XM0M87F357)
GLYCERIN (UNII: PDC6A3C0OX)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
CI 77491 (UNII: 1K09F3G675)
DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ)
MAGNESIUM SULFATE (UNII: DE08037SAB)

Product Characteristics
Color	brown	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85161-128-01	1 in 1 BOX	08/30/2025
1		1 g in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	08/30/2025

Labeler - Longway Technology(Guangzhou) Co., Ltd. (844528915)

Registrant - Longway Technology(Guangzhou) Co., Ltd. (844528915)

Establishment
Name	Address	ID/FEI	Business Operations
Longway Technology(Guangzhou) Co., Ltd.		844528915	manufacture(85161-128)