COPPERTONE TANNING SUNSCREEN SPF 15- avobenzone 2%, homosalate 5%, octisalate 4.5%, octocrylene 3% lotion

Coppertone Tanning Sunscreen SPF 15 by

Drug Labeling and Warnings

Coppertone Tanning Sunscreen SPF 15 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 2%, Homosalate 5%, Octisalate 4.5%, Octocrylene 3%

Purpose

Sunscreen

Use

■ helps prevent sunburn

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 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 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

■ 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, glycerin, silica, phenoxyethanol, isododecane, ethylhexylglycerin, polyester-27, styrene/acrylates copolymer, acrylates/C10-30 alkyl acrylate crosspolymer, arachidyl alcohol, neopentyl glycol diheptanoate, glyceryl stearate, PEG-100 stearate, tocopherol, beeswax, fragrance, behenyl alcohol, arachidyl glucoside, potassium hydroxide, disodium EDTA, sodium ascorbyl phosphate

Questions?

1-866-288-3330

PRINCIPAL DISPLAY PANEL

Coppertone ® Sunscreen Lotion

Tanning

Lightweight & Moisturizing 15

No Dyes, PABA, Oxybenzone

Water Resistant (80 Minutes)

8 FL OZ (237 mL)

INGREDIENTS AND APPEARANCE

COPPERTONE TANNING SUNSCREEN SPF 15 
avobenzone 2%, homosalate 5%, octisalate 4.5%, octocrylene 3% lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66800-4087
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	2 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.5 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	5 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
TOCOPHEROL (UNII: R0ZB2556P8)
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
SYNTHETIC BEESWAX (UNII: 08MNR5YE2R)
PEG-100 STEARATE (UNII: YD01N1999R)
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
POLYESTER-7 (UNII: 0841698D2F)
FRAGRANCE FLORAL ORC0902236 (UNII: R66Z4YW3X0)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ISODODECANE (UNII: A8289P68Y2)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
DOCOSANOL (UNII: 9G1OE216XY)
ACRYLATES CROSSPOLYMER-6 (UNII: 4GXD0Q3OS3)

Product Characteristics
Color	white (White to Off-White)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66800-4087-1	237 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/20/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	12/20/2021

Labeler - Beiersdorf Inc (001177906)