CELL FUSION C LASER UV DEFENSE SUNSCREEN BROAD SPECTRUM SPF 50- homosalate, octisalate, octocrylene, zinc oxide cream

Cell Fusion C Laser UV Defense Sunscreen Broad Spectrum SPF 50 by

Drug Labeling and Warnings

Cell Fusion C Laser UV Defense 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 6.0%
Octisalate 4.5%
Octocrylene 5.0%
Zinc Oxide 10.38%

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​ on damaged or broken skin

WHEN USING

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

STOP USE

• Stop use and ask a doctor if 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

• Apply generously and evenly 15 minutes before sun exposure.
• Reapply at least every 2 hours.
• Use a water resistant sunscreen if swimming or sweating.
• 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 this product in this container from excessive heat and direct sun.
• May stain some fabrics or surfaces.

INACTIVE INGREDIENTS

Water, Caprylic/Capric Triglyceride, Propanediol, Glycerin, Coco-Caprylate/Caprate, Cetearyl Olivate, Sphingomonas Ferment Extract, Hippophae Rhamnoides Oil, Sodium Hyaluronate, Hamamelis Virginiana (Witch Hazel) Water, Houttuynia Cordata Extract, Centella Asiatica Extract, Pentylene Glycol, 1,2-Hexanediol, Sorbitan Olivate, Glyceryl Stearate, Potassium Cetyl Phosphate, Lauroyl Lysine, Polyhydroxystearic Acid, Hydroxyacetophenone, Sodium Polyacryloyldimethyl Taurate, Acrylates Copolymer, Triethoxycaprylylsilane, Stearic Acid, Panthenol, Tromethamine, Neopentyl Glycol Diethylhexanoate, Polyacrylate Crosspolymer-6, Hydroxypropyl Methylcellulose Stearoxy Ether, Trisodium Ethylenediamine Disuccinate, Acetyl Glucosamine, Biosaccharide Gum-1, Sodium Hyaluronate Crosspolymer, Caprylyl Glycol, Hydrogenated Lecithin, Butylene Glycol, Ceramide NP, Sucrose Stearate, Palmitic Acid, Cholesterol, Ceramide NS, Glycosphingolipids, Phytosphingosine, Ceramide AP, Ceramide AS, Ethylhexylglycerin, Sodium DNA, Ceramide EOP, Cetearyl Alcohol, Fragrance (Parfum)

QUESTIONS?

Call +1-949-418-8592
Outside U.S. +82-080-889-7760
cmslab_os@wonik.com

SPL UNCLASSIFIED SECTION

Distributed By
Hansung USA LLC
15375 Barranca Parkway
Suite B-109, Irvine, CA USA 92618
CMS LAB Inc.
www.cellfusionc.com
Made in Korea

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

Cell Fusion C

LASER
UV DEFENSE
SUNSCREEN

BROAD SPECTRUM
SPF 50

FOR ALL SKIN TYPES
LIGHTWEIGHT FINISH

50 ML / 1.69 FL.OZ.

INGREDIENTS AND APPEARANCE

CELL FUSION C LASER UV DEFENSE SUNSCREEN BROAD SPECTRUM SPF 50 
homosalate, octisalate, octocrylene, zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52554-9062
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	6 g  in 50 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	5 g  in 50 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.5 g  in 50 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	10.38 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: 52554-9062-1	1 in 1 BOX	02/14/2025
1		50 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	02/14/2025

Labeler - CMS LAB Inc. (557795012)

Registrant - CMS LAB Inc. (557795012)