CELL FUSION C LASER SUNSCREEN BROAD SPECTRUM SPF 50- homosalate, octisalate, titanium dioxide, zinc oxide cream

Cell Fusion C Laser Sunscreen Broad Spectrum SPF 50 by

Drug Labeling and Warnings

Cell Fusion C Laser Sunscreen Broad Spectrum SPF 50 by is a Otc medication manufactured, distributed, or labeled by CMS LAB Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENTS

Homosalate 7.5%
Octisalate 4.5%
Titanium Dioxide 2.2%
Zinc Oxide 12.7%

PURPOSE

Sunscreen

USES

• helps prevent sunburn
• 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

DO NOT USE

• Do not use​ ondamaged or broken skin

WHEN USING

• When using this productkeep out of the eyes. Rinse with water to remove.

STOP USE

• Stop use and ask a doctorif rash occurs

KEEP OUT OF REACH OF CHILDREN

• Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS For sunscreen use:

• apply generously and evenly 15 minutes before sun exposure
• reapply:
• after 80 minutes of swimming or sweating
• immediately after towel drying
• ​at least every 2 hours
• Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:

• limit time in the sun, especially from 10 a.m.-2 p.m.
• wear long-sleeved shirts, pants, hats, and sunglasses
• children under 6 months of age: Ask a doctor

OTHER INFORMATION

• protect the product in this container from excessive heat and direct sun
• may stain some fabrics or surfaces.

INACTIVE INGREDIENTS

WATER, CYCLOPENTASILOXANE, DIPROPYLENE GLYCOL, DISILOXANE, LAURYL PEG-10 TRIS(TRIMETHYLSILOXY) SILYLETHYL DIMETHICONE, GLYCERIN, BUTYLOCTYL SALICYLATE, SILICA, DIMETHICONE, DISTEARDIMONIUM HECTORITE, MAGNESIUM SULFATE, METHYL METHACRYLATE CROSSPOLYMER, 1,2-HEXANEDIOL, TRIETHOXYCAPRYLYLSILANE, STEARIC ACID, ALUMINUM HYDROXIDE, SORBITAN CAPRYLATE, DIMETHICONE/PEG-10/15 CROSSPOLYMER, LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, GLYCERYL CAPRYLATE, ETHYLHEXYLGLYCERIN, SODIUM CITRATE, HYDROXYDECYL UBIQUINONE, HYDROLYZED COLLAGEN, TOCOPHEROL, HYDROGENATED LECITHIN, CERAMIDE NP, SUCROSE STEARATE, CHOLESTEROL, CHOLESTERYL MACADAMIATE, PALMITIC ACID, BIOSACCHARIDE GUM-4, SACCHARIDE ISOMERATE, HYDROLYZED LUPINE PROTEIN

QUESTIONS?

Call 212-804-7608
Outside U.S. +82 080-889-7760
www.cellfusionc.com

Dist. by Dkcos
20 W 33rd St New York, NY 10001
www.dkcos.com

CMS LAB Inc.

Made in Korea

PRINCIPAL DISPLAY PANEL: 50ML / 1.69 FL.OZ. Carton

Cell Fusion C

Dermatological Laboratory

LASER
SUNSCREEN
Broad Spectrum SPF 50+

Effective UV Protection
Improve Overall
Skin Condition

WATER RESISTANT
(80 minutes)

50ML / 1.69 FL.OZ.

10ML / 0.33 FL.OZ.

INGREDIENTS AND APPEARANCE

CELL FUSION C LASER SUNSCREEN BROAD SPECTRUM SPF 50 
homosalate, octisalate, titanium dioxide, zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52554-9052
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	7.5 g  in 50 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	12.7 g  in 50 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.5 g  in 50 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.2 g  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52554-9052-1	1 in 1 BOX	12/01/2024
1		50 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 52554-9052-2	1 in 1 BOX	12/01/2024
2		10 mL in 1 TUBE; 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	12/01/2024

Labeler - CMS LAB Inc. (557795012)

Registrant - CMS LAB Inc. (557795012)