COPPERTONE SUNSCREEN SPF 50- avobenzone 3%, homosalate 10%, octisalate 4.5%, octocrylene 8% lotion 
Beiersdorf Inc

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Coppertone Sport Lotion SPF 50

Drug Facts

Active ingredients

Avobenzone 3%, Homosalate 10%, Octisalate 4.5%, Octocrylene 8%

Purpose

Sunscreen

Use

■ helps prevent sunburn

Warnings

For external use only

Do not use on damaged or broken skin

Stop use and ask a doctor if rash occurs

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

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

Directions

■ apply liberally 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-sleeve shirts, pants, hats, and sunglasses

■ children under 6 months: Ask a doctor

Other information

■ protect this product from excessive heat and direct sun

■ may stain or damage some fabrics or surfaces

Inactive ingredients

water, aluminum starch octenylsuccinate, styrene/acrylates copolymer, glycerin, polyester-27, silica, phenoxyethanol,

isododecane, arachidyl alcohol, beeswax, ethylhexylglycerin, neopentyl glycol

diheptanoate, behenyl alcohol, tocopherol, acrylates/C10-30 alkyl acrylate

crosspolymer, arachidyl glucoside, glyceryl stearate, PEG-100 stearate, potassium

hydroxide, fragrance, disodium EDTA, sodium ascorbyl phosphate

Questions?

1-866-288-3330

Coppertone ® Suncreen Lotion

Sport 50

4-IN-1 Performance

Stops up to 98% UV Rays

+Resists

Sweat+Heat+Water

Free of Oxybenzone, Octinoxate, PABA, Phthalates & Dyes

Water Resistant (80 Minutes)

Broad Spectrum SPF 50

Sport FrontSport back

COPPERTONE SUNSCREEN SPF 50 
avobenzone 3%, homosalate 10%, octisalate 4.5%, octocrylene 8% lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66800-4107
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE4.5 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE8 g  in 100 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE10 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)  
PEG-20 STEARATE (UNII: NBX892EA57)  
STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)  
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)  
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
DOCOSANOL (UNII: 9G1OE216XY)  
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
GLYCERIN (UNII: PDC6A3C0OX)  
SYNTHETIC BEESWAX (UNII: 08MNR5YE2R)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
WATER (UNII: 059QF0KO0R)  
FRAGRANCE FLORAL ORC0902236 (UNII: R66Z4YW3X0)  
POLYESTER-7 (UNII: 0841698D2F)  
ISODODECANE (UNII: A8289P68Y2)  
Product Characteristics
Colorwhite (white to off-white) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66800-4107-389 g in 1 TUBE; Type 0: Not a Combination Product11/02/2020
2NDC:66800-4107-7207 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/02/2020
3NDC:66800-4107-8259 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/02/2020
4NDC:66800-4107-9269 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/02/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02011/02/2020
Labeler - Beiersdorf Inc (001177906)

Revised: 6/2024
Document Id: 1c0c3f0a-8ec3-43ed-e063-6294a90abe05
Set id: d8b0d5ad-a82c-5304-e053-2a95a90afa63
Version: 6
Effective Time: 20240629
 
Beiersdorf Inc