Surface Sun Dry Touch SPF 40 Sunscreen

Manufacturer
Surface Products Corp | CGI Packaging, LLC
Effective date
2018-05-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:55:38

Label at a glance#

ProductSurface Sun Dry Touch SPF 40 Sunscreen
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OXYBENZONE, OCTOCRYLENE
Label structure8 sections

Dosage and administration

Spray liberally and evenly by hand 15 minutes before sun exposure. Reapply after: 80 minutes of sweating or swimming immediately after towel drying at least every 2 hours Hold can 4-6 inches from the skin to apply. Do not spray directly into your face. Spray on hands an then apply to face. Do not apply in windy conditions. Use in a well-ventilated area. Sun Protection Measures: Spending time in the sun increases y...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 10%, Oxybenzone 6%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

DOSAGE & ADMINISTRATION SECTION

Helps prevent sunburn.

Warnings

WARNINGS SECTION

For external use only.

Flammable: do not use near heat, flame, or while smoking. Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse eyes with water to remove. Keep away from face to avoid breathing it. Do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120F. Stop use and ask a doctor if rash occurs.

Keep Out of Reach of Children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

INDICATIONS & USAGE SECTION

Spray liberally and evenly by hand 15 minutes before sun exposure.

Reapply after:

80 minutes of sweating or swimming

immediately after towel drying

at least every 2 hours

Hold can 4-6 inches from the skin to apply. Do not spray directly into your face. Spray on hands an then apply to face. Do not apply in windy conditions. Use in a well-ventilated area.

Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:

Limit time in the sun, especially from 10 a.m. - 2 p.m.

Wear long-sleeved shirts, pants, hats, and sunglasses.

Children under 6 months: ask a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Acrylates/Octylacrylamide Crosspolymer, Alcohol Denat., Caprylic/Capric Triglyceride, Diethylhexyl Syringylidenemalonate, Fragrance, Glycerin.

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Surface Sun Dry Touch SPF 40Surface Sun Dry Touch SPF 40

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72344-004-062020-01-31C16284748780-19d75b9cf-fac4-f424-e053-dadaa90a57ce6ce1a30c-b1b9-e112-e053-2a91aa0a1888

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72344-004-06Surface Sun Dry Touch SPF 40 Sunscreen170 mL in 1 CANSPRAY1701

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72344-004SURFACE SUN DRY TOUCH SPF 40 SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) SPRAY [SURFACE PRODUCTS CORP]1Legacy NDC, 1 package rows20180523_6ce1a30c-b1b9-e112-e053-2a91aa0a1888.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72344-00472344-004-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
6ce1846d-ddef-96a8-e053-2991aa0abf356ce1a30c-b1b9-e112-e053-2a91aa0a18882018-05-23WarningsExact identifier
spl id: 6ce1846d-ddef-96a8-e053-2991aa0abf35
spl set id: 6ce1a30c-b1b9-e112-e053-2a91aa0a1888

Reported adverse events (FAERS/openFDA)#

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