52554-9063-1 Cell Fusion C Derma UV Mineral Sunscreen Broad Spectrum SPF 50 50mL

Cell Fusion C Laser Derma UV Mineral Sunscreen Broad Spectrum SPF 50 by

Drug Labeling and Warnings

Cell Fusion C Laser Derma UV Mineral 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]

CELL FUSION C LASER DERMA UV MINERAL SUNSCREEN BROAD SPECTRUM SPF 50- homosalate, octisalate, octocrylene, zinc oxide cream 
CMS LAB Inc.

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52554-9063-1 Cell Fusion C Derma UV Mineral Sunscreen Broad Spectrum SPF 50 50mL

Drug Facts

ACTIVE INGREDIENTS

Zinc Oxide 19.0%

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​ on damaged or broken skin

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

  • Stop use and ask a doctor if rash occurs

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

DIRECTIONS

  • Apply liberally 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, Cyclohexasiloxane, Isododecane, Butyloctyl Salicylate, 2,3-Butanediol, Propylheptyl Caprylate, Caprylyl Methicone, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Magnesium Sulfate, Centella Asiatica Extract, Citrus Aurantium Dulcis (Orange) Oil, Hippophae Rhamnoides Fruit Oil, Citrus Nobilis (Mandarin Orange) Peel Oil, Sodium Hyaluronate, Litsea Cubeba Fruit Oil, Lauryl Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Disteardimonium Hectorite, Methyl Methacrylate Crosspolymer, Polymethylsilsesquioxane, Triethoxycaprylylsilane, 1,2-Hexanediol, Alumina, Polyglyceryl-2 Dipolyhydroxystearate, Propylene Carbonate, Glyceryl Caprylate, Caprylyl Glycol, Ethylhexylglycerin, Tocopherol, Panthenol, Limonene, Citral, Linalool

QUESTIONS?

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

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

DERMA
UV MINERAL
SUNSCREEN

BROAD SPECTRUM
SPF 50

SUITABLE FOR SENSITIVE SKIN
NATURAL FINISH

50 ML / 1.69 FL.OZ.

cell_fusion_c_derma_uv_mineral_sunscreen_spf50

CELL FUSION C LASER DERMA UV MINERAL SUNSCREEN BROAD SPECTRUM SPF 50 
homosalate, octisalate, octocrylene, zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 52554-9063
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE19 g  in 50 mL
Inactive Ingredients
Ingredient NameStrength
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
CITRAL (UNII: T7EU0O9VPP)  
LINALOOL (UNII: D81QY6I88E)  
2,3-BUTANEDIOL (UNII: 45427ZB5IJ)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
SODIUM HYALURONATE (UNII: YSE9PPT4TH)  
.ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)  
CYCLOHEXASILOXANE (UNII: XHK3U310BA)  
ISODODECANE (UNII: A8289P68Y2)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
LAURYL POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: H49Q67JS3B)  
WATER (UNII: 059QF0KO0R)  
CAPRYLYL METHICONE (UNII: Q95M2P1KJL)  
CENTELLA ASIATICA (UNII: 7M867G6T1U)  
POLYMETHYLSILSESQUIOXANE (UNII: 59Z907ZB69)  
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
ALUMINA (UNII: LMI26O6933)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)  
CITRUS AURANTIUM DULCIS (ORANGE) OIL (UNII: AKN3KSD11B)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
LITSEA CUBEBA FRUIT OIL (UNII: 2XIW34BN6O)  
PANTHENOL (UNII: WV9CM0O67Z)  
PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD)  
MAGNESIUM SULFATE (UNII: DE08037SAB)  
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)  
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)  
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 52554-9063-11 in 1 BOX02/14/202502/14/2025
150 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02002/14/202502/14/2025
Labeler - CMS LAB Inc. (557795012)
Registrant - CMS LAB Inc. (557795012)

Revised: 2/2025
Document Id: 2e5c58b0-8446-a187-e063-6294a90a70b7
Set id: 2dff671c-04cc-f58d-e063-6294a90a537b
Version: 2
Effective Time: 20250214
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