COCO EVE SUNNY HONEY HIGHLIGHTER BODY SPF 50- homosalate, octocrylene, octisalate, avobenzone lotion

COCO EVE SUNNY HONEY HIGHLIGHTER BODY SPF 50 by

Drug Labeling and Warnings

COCO EVE SUNNY HONEY HIGHLIGHTER BODY SPF 50 by is a Otc medication manufactured, distributed, or labeled by COSMAX USA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients

Homosalate 15%

Octocrylene 10%

Octisalate 5%

Avobenzone 3%

PURPOSE

Purpose

Sunscreen

USES

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

Warnings

For external use only.

Do not use on damaged or broken skin

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

Stop use and ask a doctor if rash occurs.

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

DIRECTIONS

Directions

• Shake well before use. Apply generously all over the body 20 minutes before sun exposure, ensuring every part of the body is covered. Reapply after 40 minutes of swimming or sweating, immediately after towel drying and 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 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

INACTIVE INGREDIENT

Inactive Ingredients: Ethylhexyl Palmitate, Diethylhexyl 2,6-Naphthalate, Butyloctyl Salicylate, Polyester-8, Dextrin Palmitate, Silica, Diethylhexyl Syringylidenemalonate, Fragrance (Parfum), Helianthus Annuus (Sunflower) Seed Oil, Tocopherol, Synthetic Fluorphlogopite, Caprylic/Capric Triglyceride, Citrullus Lanatus (Watermelon) Seed Oil, Prunus Armeniaca (Apricot) Kernel Oil, CI 77891, Cocos Nucifera (Coconut) Oil, Ananas Sativus (Pineapple) Fruit Extract, Psidium Guajava Fruit Extract, Theobroma Cacao (Cocoa) Seed Extract, CI 77491, Tin Oxide.

OTHER INFORMATION

Other Information

Protect the product from excessive heat and direct sun.

QUESTIONS?

Questions? Contact (609) 320-4845

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

COCO EVE SUNNY HONEY HIGHLIGHTER BODY SPF 50 
homosalate, octocrylene, octisalate, avobenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68577-244
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 mg  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 mg  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	10 mg  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	15 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)
SILICA (UNII: ETJ7Z6XBU4)
MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M)
ANANAS SATIVUS (PINEAPPLE) FRUIT (UNII: 2A88ZO081O)
THEOBROMA CACAO (COCOA) SEED POWDER (UNII: D9108TZ9KG)
TOCOPHEROL (UNII: R0ZB2556P8)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
CITRULLUS LANATUS (WATERMELON) SEED OIL (UNII: L33J06UQTT)
COCOS NUCIFERA (COCONUT) OIL (UNII: Q9L0O73W7L)
PSIDIUM GUAJAVA FRUIT (UNII: 74O70D6VG0)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
APRICOT KERNEL OIL (UNII: 54JB35T06A)
TIN OXIDE (UNII: KM7N50LOS6)
DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FERRIC OXIDE (UNII: 1K09F3G675)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL (UNII: 3W1JG795YI)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68577-244-01	150 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/06/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	03/06/2026

Labeler - COSMAX USA (010990210)

Registrant - COSMAX USA (010990210)

Establishment
Name	Address	ID/FEI	Business Operations
COSMAX USA		010990210	manufacture(68577-244)