FDA.reportPublic FDA data

Snappy SPF 30 Sunscreen

Manufacturer
Inspec Solutions LLC.
Effective date
2018-12-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:43:45

Label at a glance#

ProductSnappy SPF 30 Sunscreen
Active ingredientAVOBENZONE, OCTOCRYLENE, HOMOSALATE, OCTISALATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%

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.

WARNINGS SECTION

WARNINGS

For external use only.

Highly Flammable: Do not apply or use product near heat, flame, or while smoking.

OTC - PURPOSE SECTION

Avobenzone 3% ................................ Suncreen

Homosalate 15% ............................... Sunscreen

Octisalate 5% .................................... Sunscreen

Octocrylene 10% ............................... 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

Bisabolol, Caprylic /Capric Triglyceride, Cyclopentasiloxane, Ethylhexyl Palmitate, Phenlyl Trimethicone, Polyester-8, Tocopheryl Acetate, VP/Hexadecene Copolymer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Snappyscreen SPF 30Snappyscreen SPF 30

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72667-004-012020-01-31C16284748780-19d75b9d0-98b9-f424-e053-dadaa90a57ceSnappy Sunscreen SPF 30
72667-004-022020-01-31C16284748780-19d75b9d0-98b9-f424-e053-dadaa90a57ceSnappy Sunscreen SPF 30

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
72667-00472667-004-01, 72667-004-02

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
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
AVOBENZONEG63QQF2NOXACTIB
OCTOCRYLENE5A68WGF6WMACTIB
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE)UF7620L1W6IACT
PHENYL TRIMETHICONEDR0K5NOJ4RIACT
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
.BETA.-BISABOLOLLP618AV2EAIACT
CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDEFJ1H6M2JG9IACT
ETHYL PALMITATEIRD3M534ZMIACT
POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED)T9296U138PIACT
VINYLPYRROLIDONE/HEXADECENE COPOLYMERKFR5QEN0N9IACT

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
7c885105-d13a-5037-e053-2a91aa0a46817c885105-d139-5037-e053-2a91aa0a46812018-12-08WarningsExact identifier
spl id: 7c885105-d13a-5037-e053-2a91aa0a4681
spl set id: 7c885105-d139-5037-e053-2a91aa0a4681

Reported adverse events (FAERS/openFDA)#

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