POOLSIDE CLEAR INTENTIONS INVISIBLE FACE SUNSCREEN SPF 30- homosalate, octocrylene, octisalate,octinoxate, avobenzone gel

Poolside Clear Intentions Invisible Face Sunscreen SPF 30 by

Drug Labeling and Warnings

Poolside Clear Intentions Invisible Face Sunscreen SPF 30 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 10%, Octocrylene 8%, Octisalate 5% ,Octinoxate 5%, Avobenzone 3%

PURPOSE

Sunscreen

KEEP OUT OF REACH OF CHILDREN

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

QUESTIONS

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

OTHER SAFETY INFORMATION

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

DOSAGE & ADMINISTRATION

Apply gererously 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

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

INDICATIONS & USAGE

Helps prevent sunburn.

INACTIVE INGREDIENT

HYDROGENATED POLY(C6-14 OLEFIN), TRISILOXANE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, SILICA, HYDROGENATED STYRENE/ISOPRENE COPOLYMER, PHENOXYETHANOL, GLYCERYL CAPRYLATE, BHT, PENTAERYTHRITYL TETRA-DI-t-BUTYL HYDROXYHYDROCINNAMATE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

POOLSIDE CLEAR INTENTIONS INVISIBLE FACE SUNSCREEN SPF 30 
homosalate, octocrylene, octisalate,octinoxate, avobenzone gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85161-150
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	0.05 g  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	0.03 g  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	0.1 g  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	0.08 g  in 1 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
HYDROGENATED POLY(C6-14 OLEFIN; 4 CST) (UNII: 7C6HV4SSLA)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
STYRENE/ISOPRENE COPOLYMER (28:72; 210000 MW) (UNII: H58HX2GWJ5)
SILICA (UNII: ETJ7Z6XBU4)
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
BHT (UNII: 1P9D0Z171K)
PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE (UNII: 255PIF62MS)
TRISILOXANE (UNII: 9G1ZW13R0G)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85161-150-01	50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/25/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/25/2026

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(85161-150)