CLINICAL SKIN FILTER TINTED SUNSCREEN cream

Clinical Skin Filter Tinted Sunscreen by

Drug Labeling and Warnings

Clinical Skin Filter Tinted Sunscreen by is a Otc medication manufactured, distributed, or labeled by KRX RESOURCES SDN. BHD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Use fingertips and apply all over face and neck, Apply liberally before sun exposure and reapply after 60 minutes of swimming and/or sweating.

WARNINGS

Warning:
Spending time under the sun for
long period time increases your risk of skin cancer and early signs of ageing.
External Use Only.
If Irritation occurs, stop using and
consult your doctor.
Keep out of reach of children.
If product is swallowed, get medical help or contact poison control immediately.

INACTIVE INGREDIENT

Inactive Ingredients:

Water, Cyclopentasiloxane, Ethylhexyl Methoxycinnamate, Titanium Dioxide, Ethylhexyl Salicylate, Zinc Oxide, Butyloctyl Salicylate, Caprylic/Capric Triglyceride, Octocrylene, Cetyl PEG/PPG-10/1 Dimethicone,
Glycerin, Methylpropanediol, Niacinamide, 1,2- Hexanediol, Dimethicone, Disteardimonium Hectorite, Sorbitan Olivate, Sorbitan Sesquioleate, Microcrystalline Wax, Lauroyl Lysine, Magnesium Sulfate, PEG-30 Dipolyhydroxystearate, Quaternium-18 Bentonite, CI 77492, Silica, Triethoxycaprylylsilane, CI 77491, Crataegus Cuneata Fruit Extract, Prunus Persica (Peach) Fruit Extract, Pyrus Communis (Pear) Fruit Extract, Ethylhexylglycerin, CI 77499, Adenosine, Hedera Helix (Ivy) Extract, Vanilla Planifolia Fruit Extract, Musa Sapientum (Banana) Fruit Extract, Disodium EDTA, BHT, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate.

INDICATIONS & USAGE

Our CLINICAL SKIN FILTER Mineral Tinted Sunscreen does not leave a white cast, dries on matte, blurs the pores and just leaves skin smooth and photo ready!
The tint blends in, and It feels like a second skin, It is also water resistant, and helps skin recover from existing sun damage.
It can be used under make up without leaving clumped and patchy areas. This product is really like no other, and you will love every application.
-Pore Blurring -Ultra Matte
-Non Comedogenic
-White Cast cancellation -Picture perfect
CRUELTY FREE.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

PURPOSE

FOR ALL SKIN TYPES WATER & SWEAT RESISTANT (60 MINUTES)

CLINICAL SKIN FILTER Mineral Tinted Sunscreen
TRANSLUCENT Light/Medium

Directions:
Use fingertips and apply all over face and neck, Apply liberally before sun exposure and reapply after 60
minutes of swimming and/or sweating.

ACTIVE INGREDIENT

Active:
Cyclopentasiloxane -8%
Titanium Dioxide - 5.78%
Zinc Oxide - 3.94%
Octocrylene -3%

PRINCIPAL DISPLAY PANEL

CLINICAL SKIN FILTER Mineral Tinted Sunscreen TRANSLUCENT Light/Medium

INGREDIENTS AND APPEARANCE

CLINICAL SKIN FILTER TINTED SUNSCREEN 
clinical skin filter tinted sunscreen cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84755-0003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	1.182 mg  in 30 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1.734 mg  in 30 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	0.9 mg  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
METHYLPROPANEDIOL (UNII: N8F53B3R4R)
NIACINAMIDE (UNII: 25X51I8RD4)
PENTAMETHYL CYCLOPENTASILOXANE (UNII: K29QC5YCW8)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
SORBITAN OLIVATE (UNII: MDL271E3GR)
MAGNESIUM DISODIUM EDTA (UNII: NDT563S5VZ)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
CRATAEGUS CUNEATA FRUIT (UNII: 98TEA9T639)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
DIMETHICONE 100 (UNII: RO266O364U)
QUATERNIUM-18 (UNII: O7757NO1VL)
PYRUS COMMUNIS WHOLE (UNII: 80UKV9Y4B3)
HEDERA HELIX LEAF (UNII: ZP9XFG71A7)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
LAUROYL LYSINE (UNII: 113171Q70B)
POTASSIUM MAGNESIUM SULFATE (UNII: YI4N487572)
GLYCERIN (UNII: PDC6A3C0OX)
PRUNUS PERSICA FRUITING TOP (UNII: U08429QT99)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
VANILLA PLANIFOLIA WHOLE (UNII: BOS0R5Y21O)
WATER (UNII: 059QF0KO0R)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84755-0003-1	30 mL in 1 PACKAGE; Type 0: Not a Combination Product	09/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/01/2024

Labeler - KRX RESOURCES SDN. BHD. (813058498)

Registrant - KRX RESOURCES SDN. BHD. (813058498)

Establishment
Name	Address	ID/FEI	Business Operations
KRX RESOURCES SDN. BHD.		813058498	manufacture(84755-0003)