FDA.reportPublic FDA data

Poolside Butter SCREEN SPF 30 sunscreen Butter

Manufacturer
Longway Technology(Guangzhou)Co.,Ltd.
Effective date
2025-12-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:33:09

Label at a glance#

ProductPoolside Butter SCREEN SPF 30 sunscreen Butter
Active ingredientOCTISALATE, AVOBENZONE, HOMOSALATE, OCTOCRYLENE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

Helps prevent sunburn.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - QUESTIONS SECTION

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

DOSAGE & ADMINISTRATION SECTION

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.

WARNINGS SECTION

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 m on damaged or broken skin.
When using this product keep out of eves. rinse with water to remove
Stop use and ask 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.

OTHER SAFETY INFORMATION

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

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Poolside Butter SCREEN SPF 30 sunscreen ButterPoolside Butter SCREEN SPF 30 sunscreen Butter

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85161-165-01Poolside Butter SCREEN SPF 30 sunscreen Butter80 g in 1 BOTTLEOIL801

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85161-16585161-165-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
FRAGRANCE 135765EM498GW35IACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
SILICAETJ7Z6XBU4IACT
EDETATE DISODIUM7FLD91C86KIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
OCTISALATE4X49Y0596WACTIB
AVOBENZONEG63QQF2NOXACTIB
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL724GKU717MIACT
ALLANTOIN344S277G0ZIACT
METHICONE (20 CST)6777U11MKTIACT
XANTHAN GUMTTV12P4NEEIACT
PEG-100 STEARATEYD01N1999RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
WATER059QF0KO0RIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
HOMOSALATEV06SV4M95SACTIB
TREHALOSEB8WCK70T7IIACT
OCTOCRYLENE5A68WGF6WMACTIB
POTASSIUM CETYL PHOSPHATE03KCY6P7UTIACT
COCOS NUCIFERA (COCONUT) OILQ9L0O73W7LIACT
BUTYROSPERMUM PARKII (SHEA) BUTTERK49155WL9YIACT
BEHENYL ALCOHOL9G1OE216XYIACT
GLYCERYL STEARATE230OU9XXE4IACT
1,2-HEXANEDIOLTR046Y3K1GIACT
CETEARYL ALCOHOL2DMT128M1SIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Poolside Butter SCREEN SPF 30 sunscreen ButterHOMOSALATE , OCTOCRYLENE , OCTISALATE , AVOBENZONELongway Technology(Guangzhou)Co.,Ltd.452bd24d-8654-e6c0-e063-6394a90a0aea2025-12-04WarningsExact identifier
ndc (package): 85161-165-01
ndc (product): 85161-165
ndc11 (package): 85161016501
spl id: 452bd24d-8655-e6c0-e063-6394a90a0aea
spl set id: 452bd24d-8654-e6c0-e063-6394a90a0aea

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.