COPPERTONE EVERY TONE INVISIBLE CLEAR SUNSCREEN STICK SPF 55- avobenzone 3%, homosalate 10%, octisalate 5%, octocrylene 10% stick

Coppertone Every Tone Invisible Clear Sunscreen Stick SPF 55 by

Drug Labeling and Warnings

Coppertone Every Tone Invisible Clear Sunscreen Stick SPF 55 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 10%,
Octisalate 5%, Octocrylene 10%

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 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 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-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

octyldodecanol, dicaprylyl carbonate, dicaprylyl ether, butylene glycol dicaprylate/dicaprate, butyloctyl salicylate, isopropyl
palmitate, neopentyl glycol diheptanoate, silica dimethyl silylate, dibutyl lauroyl glutamide, bis-octyldodecyl dimer dilinoleate/propanediol copolymer, dibutyl ethylhexanoyl glutamide, polyamide-8, silica, ethylcellulose, hydroxyacetophenone, ceramide NP, phytosphingosine, oleic acid

Questions?

1-866-288-3330

PRINCIPAL DISPLAY PANEL

NEW

Coppertone ® Clear Sunscreen Stick

Developed with Dermatologists

Transparent on all skin tones

Won't clog pores

Broad Spectrum SPF 55

NET WT 0.49 OZ (13.9 g)

INGREDIENTS AND APPEARANCE

COPPERTONE EVERY TONE INVISIBLE CLEAR SUNSCREEN STICK SPF 55 
avobenzone 3%, homosalate 10%, octisalate 5%, octocrylene 10% stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66800-8003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	10 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
CALCIUM SILICATE (UNII: S4255P4G5M)
ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
OCTYLDODECANOL (UNII: 461N1O614Y)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
BIS-OCTYLDODECYL DIMER DILINOLEATE/PROPANEDIOL COPOLYMER (UNII: TY3J98ZR7R)
POLYAMIDE-8 (4500 MW) (UNII: 77723GV81A)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
OLEIC ACID (UNII: 2UMI9U37CP)
DIBUTYL LAUROYL GLUTAMIDE (UNII: 3V7K3IA58X)
BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI)
CERAMIDE NP (UNII: 4370DF050B)
DIBUTYL ETHYLHEXANOYL GLUTAMIDE (UNII: 0IAF2L30VS)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66800-8003-1	1 in 1 CARTON	10/31/2024
1		13.9 g in 1 CANISTER; 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	10/31/2024

Labeler - Beiersdorf Inc (001177906)