Drive Sunscreen SPF 50

Manufacturer
Inspec Solutions LLC.
Effective date
2018-12-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:44:06

Label at a glance#

ProductDrive Sunscreen SPF 50
Active ingredientOCTOCRYLENE, AVOBENZONE, HOMOSALATE, OCTISALATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%

Humosalate 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% ........................Sunscreen

Humosalate 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

Alcohol Denate, Acrylates/Octylacrylamide Copolymer, Stearoxytrimethylsilane, Aloe Barbadensis Leaf Extract, Retinyl Palmitate, Tocopherol, Glycerin, Caprylic/Capric Triglyceride, Diethylhexyl Syringylidenemalonate, Fragrace.

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drive Sunscreen SPF 50Drive Sunscreen SPF 50

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72667-003DRIVE SUNSCREEN SPF 50 (AVOBENZONE, HUMOSALATE, OCTISALATE, OCTOCRYLENE) SPRAY [INSPEC SOLUTIONS LLC.]1Legacy NDC20181208_7c5e581f-1991-a172-e053-2a91aa0a27e8.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72667-00372667-003-01, 72667-003-02, 72667-003-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

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
49eb6eb2-4271-59d0-e063-6294a90a7f5d7c5e581f-1991-a172-e053-2a91aa0a27e82026-02-03WarningsExact identifier
spl set id: 7c5e581f-1991-a172-e053-2a91aa0a27e8

Reported adverse events (FAERS/openFDA)#

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