COPPERTONE EVERYTONE SUNSCREEN SPF 50- avobenzone 3%, homosalate 9%, octisalate 4.5%, octocrylene 9% spray

Coppertone EveryTone Sunscreen SPF 50 by

Drug Labeling and Warnings

Coppertone EveryTone Sunscreen SPF 50 by is a Otc medication manufactured, distributed, or labeled by Beiersdorf Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Avobenzone 3%, Homosalate 9%, Octisalate 4.5%, Octocrylene 9%

Purpose

Sunscreen

Use

■ helps prevent sunburn

Warnings

For external use only
Flammable: Do not use near heat, flame, or while smoking

DO NOT USE

Do not use on damaged or broken skin

WHEN USING

When using this product
■ keep away from face to avoid breathing it

■ keep out of eyes. Rinse with water to remove.

■ use only as directed. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

■ do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120˚F.

STOP USE

Stop use and ask a doctor if rash occurs

KEEP OUT OF REACH OF CHILDREN

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

Directions

■ shake well before each use

■ spray liberally and spread evenly by hand 15 minutes before sun exposure

■ hold container 4 to 6 inches from the skin to apply

■ do not spray directly into face. Spray on hands then apply to face.

■ do not apply in windy conditions

■ use in a well-ventilated area

■ 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

■ store between 20° to 25°C (68° to 77°F)

■ may stain or damage some fabrics or surfaces

Inactive ingredients

water, isobutane, SD alcohol 40-B (7.1% v/v), butyloctyl salicylate, diethylhexyl carbonate, glycereth-26, styrene/acrylates copolymer, butylene glycol, diisopropyl adipate, dimethicone, polyamide-8, isododecane, 1,2-hexanediol, ammonium acryloyldimethyltaurate/beheneth-25 methacrylate crosspolymer, glycerin, aloe barbadensis leaf juice, tocopherol (vitamin E), sodium ascorbyl phosphate, hydroxyacetophenone, ethylhexyl methoxycrylene, arachidyl alcohol, xanthan gum, behenyl alcohol, arachidyl glucoside, disodium EDTA

Questions?

1-866-288-3330

PRINCIPAL DISPLAY PANEL

Coppertone ® Senscreen Lotin Spray

EveryTone

Blends Clear on All Skin Tones

50

No White Residue

Hydrates for Radiant Skin

with Aloe & Nourishing Vitamin E

Free of Oxybenzone, Octinoxate,

PABA, and Phthalates

Water Resistant (80 Minutes)

Broad Spectrum SPF 50

INGREDIENTS AND APPEARANCE

COPPERTONE EVERYTONE SUNSCREEN SPF 50 
avobenzone 3%, homosalate 9%, octisalate 4.5%, octocrylene 9% spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66800-5049
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.5 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	9 g  in 100 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	9 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
POLYAMIDE-8 (4500 MW) (UNII: 77723GV81A)
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
TOCOPHEROL (UNII: R0ZB2556P8)
XANTHAN GUM (UNII: TTV12P4NEE)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
GLYCERETH-26 (UNII: NNE56F2N14)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
DOCOSANOL (UNII: 9G1OE216XY)
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
WATER (UNII: 059QF0KO0R)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
ALCOHOL (UNII: 3K9958V90M)
DIETHYLHEXYL CARBONATE (UNII: YCD50O0Z6L)
ISODODECANE (UNII: A8289P68Y2)
ISOBUTANE (UNII: BXR49TP611)
STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)
DIMETHICONE (UNII: 92RU3N3Y1O)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/BEHENETH-25 METHACRYLATE CROSSPOLYMER (52000 MPA.S) (UNII: LZ291VH90H)

Product Characteristics
Color	white (clear to white)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66800-5049-5	142 g in 1 CAN; Type 0: Not a Combination Product	11/03/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	11/03/2023

Labeler - Beiersdorf Inc (001177906)