FDA.reportPublic FDA data

SUNSCREEN GLOWING

Manufacturer
Aopline Biotechnology (Guangzhou) Co., Ltd.
Effective date
2026-01-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:32:02

Label at a glance#

ProductSUNSCREEN GLOWING
Active ingredientOCTOCRYLENE, OCTISALATE, HOMOSALATE, AVOBENZONE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

AVOBENZONE G63QQF2NOX 3.0%
OCTISALATE 4X49Y0596W 5.0%
OCTOCRYLENE 5A68WGF6WM 7.0%
HOMOSALATE V06SV4M95S 9%

OTC - PURPOSE SECTION

Sunscreen

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. lf swallowed, get medical help or contact a Poison ControlCenter right away

WARNINGS SECTION

For external use only. Do not use on damagedor broken skin.
When using this product keep out of eyes.nse 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 contact a Poison ControlCenter right away

DOSAGE & ADMINISTRATION SECTION

Apply liberally 15 minutes before sun exposure.

Reapply: at least every 2 hours or after 80 minutes of swimming or sweating.

INDICATIONS & USAGE SECTION

Directions
Apply liberally 15 minutes before sun exposure. Reapply: at least every 2 hours or after 80 minutes of swimming or sweating. Sun Protection Measures: $pending time in the sun increases your risk of skin cancer andearly skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPfof 15 or higher and other sun protection measures including: limit time in the sun, especiallyfrom 10 a.m.-2 pm, and wear long-sleeved shirts, pants, hats, and sunglasses. Childrenunder 6 months of age ask a doctor.

INACTIVE INGREDIENT SECTION

WATER
BUTYLOCTYL SALICYLATE
NEOPENTYL GLYCOL DIHEPTANOATE
MICA
CI 77891
BUTYL METHOXYDIBENZOYLMETHANE
GLYCERIN
PROPYLENE GLYCOL
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER
CETEARYL ALCOHOL
COCO-GLUCOSIDE
GLYCERYL STEARATE
PEG-100 STEARATE
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER
SILICA
POTASSIUM CETYL PHOSPHATE
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER
CETEARYL ALCOHOL
HYDROXYACETOPHENONE
PHENOXYETHANOL
ETHYLHEXYLGLYCERIN
CI 77492
TRIETHOXYCAPRYLYLSILANE
DISODIUM EDTA
CI 77491
CI 77499

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87283-006-01SUNSCREEN GLOWING60 mL in 1 BOTTLELOTION601

Products#

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

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87283-00687283-006-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTOCRYLENE5A68WGF6WMACTIB
POTASSIUM CETYL PHOSPHATE03KCY6P7UTIACT
EDETATE DISODIUM7FLD91C86KIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE)H895X08VNQIACT
CI 7789115FIX9V2JPIACT
SILICAETJ7Z6XBU4IACT
MICAV8A1AW0880IACT
GLYCERINPDC6A3C0OXIACT
COCO GLUCOSIDEICS790225BIACT
GLYCERYL STEARATE230OU9XXE4IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMERW59H9296ZGIACT
CI 774911K09F3G675IACT
PHENOXYETHANOLHIE492ZZ3TIACT
OCTISALATE4X49Y0596WACTIB
HOMOSALATEV06SV4M95SACTIB
NEOPENTYL GLYCOL DIHEPTANOATE5LKW3C543XIACT
CI 77492EX438O2MRTIACT
PEG-100 STEARATEYD01N1999RIACT
AVOBENZONEG63QQF2NOXACTIB
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
WATER059QF0KO0RIACT
FERROSOFERRIC OXIDEXM0M87F357IACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER9NH1UDD2RRIACT

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
SUNSCREEN GLOWINGAVOBENZONE ,OCTISALATE ,OCTOCRYLENE , HOMOSALATEAopline Biotechnology (Guangzhou) Co., Ltd.47df0de5-012a-c896-e063-6394a90a9cef2026-01-08WarningsExact identifier
ndc (package): 87283-006-01
ndc (product): 87283-006
ndc11 (package): 87283000601
spl id: 47df0de5-012b-c896-e063-6394a90a9cef
spl set id: 47df0de5-012a-c896-e063-6394a90a9cef

Reported adverse events (FAERS/openFDA)#

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