POOLSIDE GLOW BUTTER SCREEN SPF 30 SHIMMER SUNSCREEN BUTTER- homosalate , octocrylene, octisalate , avobenzone oil

Poolside Glow Butter Screen SPF 30 Shimmer sunscreen Butter by

Drug Labeling and Warnings

Poolside Glow Butter Screen SPF 30 Shimmer sunscreen Butter by is a Otc medication manufactured, distributed, or labeled by Longway Technology(Guangzhou)Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Homosalate 15%, Octocrylene 10%, Octisalate 5% , Avobenzone 3%

PURPOSE

Sunscreen

DOSAGE & ADMINISTRATION

Apply generously and evenly 15 minutes before sun exposure.

Reapply at least every 2hours.

Use a water resistant sunscreen if swimming or sweating.m

Children under 6 month: ask a doctor.

QUESTIONS

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

OTHER SAFETY INFORMATION

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

WARNINGS

For extetnal 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.

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

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

Helps prevent sunburn.

INACTIVE INGREDIENT

WATER，PROPYLENE GLYCOL，BEHENYL ALCOHOL，GLYCERYL STEARATE，CETEARYL ALCOHOL，PEG-100 STEARATE，CALCIUM ALUMINUM BOROSILICATE，1,2-HEXANEDIOL，PHENOXYETHANOL，FRAGRANCE，POTASSIUM CETYL PHOSPHATE，SILICA，XANTHAN GUM，SYNTHETIC FLUORPHLOGOPITE，TREHALOSE，SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL，TOCOPHERYL ACETATE，COCOS NUCIFERA (COCONUT) OIL，BUTYROSPERMUM PARKII (SHEA) BUTTER，ETHYLHEXYLGLYCERIN，DISODIUM EDTA，ALLANTOIN，METHICONE，TIN OXIDE，TITANIUM DIOXIDE(CI 77891)，IRON OXIDES(CI 77491)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

POOLSIDE GLOW BUTTER SCREEN SPF 30 SHIMMER SUNSCREEN BUTTER 
homosalate , octocrylene, octisalate , avobenzone oil

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85161-166
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	0.03 g  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	0.15 g  in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	0.05 g  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	0.1 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
BEHENYL ALCOHOL (UNII: 9G1OE216XY)
PEG-100 STEARATE (UNII: YD01N1999R)
CI 77891 (UNII: 15FIX9V2JP)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CI 77491 (UNII: 1K09F3G675)
CALCIUM ALUMINUM BOROSILICATE (UNII: 3JRB8A35M0)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
XANTHAN GUM (UNII: TTV12P4NEE)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
SILICA (UNII: ETJ7Z6XBU4)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
FRAGRANCE 13576 (UNII: 5EM498GW35)
METHICONE (20 CST) (UNII: 6777U11MKT)
TREHALOSE (UNII: B8WCK70T7I)
MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M)
COCOS NUCIFERA (COCONUT) OIL (UNII: Q9L0O73W7L)
BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)
WATER (UNII: 059QF0KO0R)
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL (UNII: 724GKU717M)
ALLANTOIN (UNII: 344S277G0Z)
TIN OXIDE (UNII: KM7N50LOS6)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85161-166-01	80 g in 1 BOTTLE; Type 0: Not a Combination Product	01/15/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/15/2026

Labeler - Longway Technology(Guangzhou)Co.,Ltd. (844528915)

Registrant - Longway Technology(Guangzhou)Co.,Ltd. (844528915)

Establishment
Name	Address	ID/FEI	Business Operations
Longway Technology(Guangzhou)Co.,Ltd.		844528915	manufacture(85161-166)