SUNSCREEN SETTING SPRITZ, SPF 45- sunscreen setting spray spray

SUNSCREEN SETTING SPRITZ, SPF 45 by

Drug Labeling and Warnings

SUNSCREEN SETTING SPRITZ, SPF 45 by is a Otc medication manufactured, distributed, or labeled by Aopline Biotechnology (Guangzhou) Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

AVOBENZONE G63QQF2NOX 2.9%
OCTISALATE 4X49Y0596W 4.9%
OCTOCRYLENE 5A68WGF6WM 9.5%

PURPOSE

Sunscreen+ Setting Spritz

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.lf swallowed, get medical help or contacta Poison Control Center right away

INDICATIONS & USAGE

Sun Protection Measures, Spending time in the sun increases your riskof skan cancer and early skin aging. lo decrease this risk, regularly use asunscreen with a Broad Spectrum SPF value of 15 or higher and other sunprotection measures including, limit time in sun, especiallv from 10 a.m.-2p.m, and wear long-sleeved shirts, pants, hats, and sunalasses. Chitdrenunder 6 months of age: ask a doctor.

DOSAGE & ADMINISTRATION

Apply liberally 15 minutes before sun exposure. Reaooly. at least every 2 hours or after 80 minutes ofswimming or sweating.

INACTIVE INGREDIENT

WATER
BHT
ALCOHOL
PEG-400
PROPYLENE GLYCOL LAURATE

WARNINGS

Warnings
For external use only 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 swallowed, get medical help or contacta Poison Control Center right away
Flammable. Do not spray near heat sparks, sources of ignition, or flames

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SUNSCREEN SETTING SPRITZ, SPF 45 
sunscreen setting spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87283-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	5.7 g  in 60 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	2.94 g  in 60 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	1.74 g  in 60 mL

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL MONOLAURATE (UNII: 668Z5835Z3)
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
BHT (UNII: 1P9D0Z171K)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87283-005-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/08/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/08/2026

Labeler - Aopline Biotechnology (Guangzhou) Co., Ltd. (514879104)

Registrant - Aopline Biotechnology (Guangzhou) Co., Ltd. (514879104)