POOLSIDE BUTTER SCREEN SPF 30 SUNSCREEN BUTTER- homosalate, octocrylene, octisalate, avobenzone liquid

Poolside Butter Screen SPF 30 Sunscreen Butter by

Drug Labeling and Warnings

Poolside Butter Screen SPF 30 Sunscreen Butter 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 15%, Octocrylene 10%, 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 doctor if

• rash occurs.

Keep out of reach of children.

• If product is swallowed get medical help or contact a poison control center right away.

Directions

• Apply generously and evenly 15 minutes before sun exposure.
• 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

WATER, PROPYLENE GLYCOL, BEHENYL ALCOHOL, GLYCERYL STEARATE, CETEARYL ALCOHOL, PEG-100 STEARATE, 1,2-HEXANEDIOL, PHENOXYETHANOL, FRAGRANCE, POTASSIUM CETYL PHOSPHATE, SILICA, XANTHAN GUM, TREHALOSE, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, TOCOPHERYL ACETATE, COCOS NUCIFERA (COCONUT) OIL, BUTYROSPERMUM PARKII (SHEA) BUTTER, ETHYLHEXYLGLYCERIN, DISODIUM EDTA, ALLANTOIN, METHICONE.

Questions or comments?

1-212- 244-5170 info@amora.beauty

Package Labeling:

INGREDIENTS AND APPEARANCE

POOLSIDE BUTTER SCREEN SPF 30 SUNSCREEN BUTTER 
homosalate, octocrylene, octisalate, avobenzone liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85179-015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	150 mg  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	100 mg  in 1 g
OCTISALATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DOCOSANOL (UNII: 9G1OE216XY)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
PEG-100 MONOSTEARATE (UNII: YD01N1999R)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
XANTHAN GUM (UNII: TTV12P4NEE)
TREHALOSE (UNII: B8WCK70T7I)
JOJOBA OIL (UNII: 724GKU717M)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
COCONUT OIL (UNII: Q9L0O73W7L)
SHEA BUTTER (UNII: K49155WL9Y)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ALLANTOIN (UNII: 344S277G0Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85179-015-00	80 g 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)