CELL FUSION C AQUATICA UV DEFENSE SUNSCREEN BROAD SPECTRUM SPF 50- avobenzone, homosalate, octisalate, octocrylene cream

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

Drug Labeling and Warnings

Cell Fusion C Aquatica 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]

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Drug Facts

ACTIVE INGREDIENTS

Avobenzone 3.0%
Homosalate 7.3%
Octisalate 5.0%
Octocrylene 9.0%

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

• 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, Propanediol, Butyloctyl, Salicylate, Ethylhexyl Methoxycrylene, Nylon-12, Silica, Sodium Acrylates Crosspolymer-2, 1,2-Hexanediol, Pentylene Glycol, Houttuynia Cordata Extract, Melia Azadirachta Leaf Extract, Melia Azadirachta Flower Extract, Sodium Hyaluronate, Cryptomeria Japonica Leaf Extract, Nelumbo Nucifera Leaf Extract, Saccharomyces Ferment, Coccinia Indica Fruit Extract, Amber Powder, Solanum Melongena (Eggplant) Fruit Extract, Curcuma Longa (Turmeric) Root Extract, Cynanchum Atratum Extract, Ocimum Sanctum Leaf Extract, Corallina Officinalis Extract, Moringa Oleifera Seed Oil, Althaea Rosea Flower Extract, Hydrolyzed Hyaluronic Acid, Hyaluronic Acid, Chlorella Vulgaris Extract, Camellia Sinensis Leaf Extract, Mentha Rotundifolia Leaf Extract, Thymus Vulgaris (Thyme) Leaf Extract, Centella Asiatica Extract, Polyglyceryl-3 Distearate, Hydroxyethyl Urea, Cetearyl Olivate, Potassium Cetyl Phosphate, Butylene Glycol, Sorbitan Olivate, Glycerin, Panthenol, Glyceryl Stearate Citrate, Ethylhexylglycerin, Acetyl Glucosamine, Hydroxyacetophenone, Sodium Hyaluronate Crosspolymer, Tocopherol, Dimethylsilanol Hyaluronate, Hydrolyzed Sodium Hyaluronate, Caprylyl Glycol, Potassium Hyaluronate, Hydroxypropyltrimonium Hyaluronate, Sodium Hyaluronate Dimethylsilanol, Sodium Acetylated Hyaluronate, Sodium DNA, Cetyl Alcohol, Carbomer, Xanthan Gum, Disodium EDTA, Fragrance (Parfum)

QUESTIONS?

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

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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

AQUATICA
UV DEFENSE
SUNSCREEN

BROAD SPECTRUM
SPF 50

FOR ALL SKIN TYPES
SHEER FINISH

50 ML / 1.69 FL.OZ.

INGREDIENTS AND APPEARANCE

CELL FUSION C AQUATICA UV DEFENSE SUNSCREEN BROAD SPECTRUM SPF 50 
avobenzone, homosalate, octisalate, octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52554-9061
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	7.3 g  in 50 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	9 g  in 50 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 50 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 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: 52554-9061-1	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)