FDA.reportPublic FDA data

SnappyScreen SPF 40

Manufacturer
Inspec Solutions
Effective date
2022-06-26
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
legacy-cache
Hydrated at
2026-08-01 21:58:04

Label at a glance#

ProductSnappyScreen SPF 40
Active ingredientHOMOSALATE, OCTOCRYLENE, AVOBENZONE, OCTISALATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Avobenzone 3.0%

Homosalate 15%

Octisalate 5%

Octocrylene 10%

OTC - WHEN USING SECTION

When using this product:

• keep out of eyes. Rinse with water to remove.

• Keep away from face to avoid breathing it.

• Do not puncture or incinerate, Contents under pressure

• Do not store at temperature above 120⁰F

Stop use and ask a doctor if rash occurs.

OTC - PURPOSE SECTION

Avobenzone 3.0% ……………………………………………………………………………… Sunscreen

Homosalate 15.0% ……………………………………………………………………………. Sunscreen

Octisalate 5.0% …………………………………………………………………………………. Sunscreen

Octocrylene 10.0% ……………………………………………………………………………. Sunscreen

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT SECTION

Behenyl Alcohol

BHT

Butyloctyl Salicylate

Caprylyl Methicone Dimethicone

Dimethyl Capramide

Disodium EDTA

Ethylhexyl Stearate

Ethylhexylglycerin

Fragrance

Glyceryl Stearate Hydrated Silica

PEG-100 Stearate

Phenoxyethanol

Polyester-8

Sodium Polyacrylate

Styrene/Acrylates Copolymer

Trideceth-6

Trimethylsiloxysilicate

VP/Hexadecene Copolymer

Water

Xanthan Gum

OTC - WHEN USING SECTION

• keep out of eyes. Rinse with water to remove.

• Keep away from face to avoid breathing it.

• Do not puncture or incinerate, Contents under pressure

• Do not store at temperature above 120⁰F

Stop use and ask a doctor if rash occurs.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SnappyScreen SPF 40SnappyScreen SPF 40

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72667-04472667-044-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
LEVOMENOL24WE03BX2TIACT
CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDEFJ1H6M2JG9IACT
CYCLOMETHICONE 50THT5PCI0RIACT
ETHYLHEXYL PALMITATE2865993309IACT
POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED)T9296U138PIACT
VINYLPYRROLIDONE/HEXADECENE COPOLYMERKFR5QEN0N9IACT
TOCOPHEROLR0ZB2556P8IACT
HOMOSALATEV06SV4M95SACTIB
OCTOCRYLENE5A68WGF6WMACTIB
AVOBENZONEG63QQF2NOXACTIB
OCTISALATE4X49Y0596WACTIB
PHENYL TRIMETHICONEDR0K5NOJ4RIACT

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
e261b239-b614-f2ee-e053-2995a90aa2abe261b1f7-77ce-4f81-e053-2995a90a55662022-06-26Exact identifier
spl id: e261b239-b614-f2ee-e053-2995a90aa2ab
spl set id: e261b1f7-77ce-4f81-e053-2995a90a5566

Reported adverse events (FAERS/openFDA)#

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