POOLSIDE SUN DAZE BODY ILLUMINATOR SPF 30 SHIMMER SUNSCREEN- homosalate, octocrylene, octisalate, avobenzone gel

Poolside Sun Daze Body Illuminator SPF 30 Shimmer Sunscreen by

Drug Labeling and Warnings

Poolside Sun Daze Body Illuminator SPF 30 Shimmer Sunscreen by is a Otc medication manufactured, distributed, or labeled by I World LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Homosalate 10%, Octocrylene 6%, Octisalate 5%, Avobenzone 3%

Purpose

Sunscreen

Uses

• Helps prevent sunburn.

Warnings

For external use only.
Skin cancer/skin aging alert

• Spending time in the sun increases your risk of skin cancer and early skin aging.
• This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.

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 product is swallowed get medical help or contact a poison control centre right away.

Directions

• Apply generously and evenly 15 minutes before sun exposer.
• Reapply at least every 2 hours.
• Use a water resistant sunscreen if swimming or sweating.
• Children under 6 month: ask a doctor.

Other information

Protect the product in this container from excessive heat and direct sun.

Inactive ingredients

MINERAL OIL (PARAFFINUM LIQUIDUM), HYDROGENATED STYRENE/ISOPRENE COPOLYMER, SILICA DIMETHYL SILYLATE, GLYCERYL CAPRYLATE, FRAGRANCE, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, SQUALANE, MACADAMIA INTEGRIFOLIA SEED OIL, OLEA EUROPAEA (OLIVE) FRUIT OIL, PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE, SYNTHETIC FLUORPHLOGOPITE, MICA, TIN OXIDE, IRON OXIDES (CI 77491), TITANIUM DIOXIDE (CI 77891), FD&C YELLOW NO. 5 (CI 19140), FD&C RED NO. 40 (CI 16035).

Questions or comments?

1-212-244-5170 info@amora.beauty

Package Labeling:

INGREDIENTS AND APPEARANCE

POOLSIDE SUN DAZE BODY ILLUMINATOR SPF 30 SHIMMER SUNSCREEN 
homosalate, octocrylene, octisalate, avobenzone gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85179-042
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	100 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	60 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
MINERAL OIL (UNII: T5L8T28FGP)
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
JOJOBA OIL (UNII: 724GKU717M)
SQUALANE (UNII: GW89575KF9)
MACADAMIA INTEGRIFOLIA SEED OIL (UNII: 7VK9GL8RUP)
OLIVE OIL (UNII: 6UYK2W1W1E)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M)
MICA (UNII: V8A1AW0880)
STANNIC OXIDE (UNII: KM7N50LOS6)
FERRIC OXIDE RED (UNII: 1K09F3G675)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 40 (UNII: WZB9127XOA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85179-042-00	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/17/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	12/17/2025

Labeler - I World LLC (830590126)

Registrant - I World LLC (830590126)