FDA.reportPublic FDA data

SUNSCREEN GLOWING, SPF 30

Manufacturer
FSA Store Inc
Effective date
2025-12-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:29:38

Label at a glance#

ProductSUNSCREEN GLOWING, SPF 30
Active ingredientOCTISALATE, AVOBENZONE, HOMOSALATE, OCTOCRYLENE
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 damaged !i or broken skin.
When using this product keep out of eyes.Rise 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
81522-220-01SUNSCREEN GLOWING, SPF 3050 mL in 1 BOTTLELOTION501

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81522-22081522-220-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

Name, UNII, Kind table
NameUNIIKind
EDETATE DISODIUM7FLD91C86KIACT
POTASSIUM CETYL PHOSPHATE03KCY6P7UTIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
PHENOXYETHANOLHIE492ZZ3TIACT
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMERW59H9296ZGIACT
MICAV8A1AW0880IACT
COCO GLUCOSIDEICS790225BIACT
SILICAETJ7Z6XBU4IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
OCTISALATE4X49Y0596WACTIB
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE)H895X08VNQIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER9NH1UDD2RRIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CI 7789115FIX9V2JPIACT
GLYCERYL STEARATE230OU9XXE4IACT
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
CI 77492EX438O2MRTIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
NEOPENTYL GLYCOL DIHEPTANOATE5LKW3C543XIACT
OCTOCRYLENE5A68WGF6WMACTIB
PEG-100 STEARATEYD01N1999RIACT
CI 77499XM0M87F357IACT
CI 774911K09F3G675IACT

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 GLOWING, SPF 30SUNSCREEN GLOWING LOTIONFSA Store Inc473bcb90-ab7f-170b-e063-6294a90a99d52025-12-31WarningsExact identifier
ndc (package): 81522-220-01
ndc (product): 81522-220
ndc11 (package): 81522022001
spl id: 473bcb90-ab80-170b-e063-6294a90a99d5
spl set id: 473bcb90-ab7f-170b-e063-6294a90a99d5

Reported adverse events (FAERS/openFDA)#

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